ENST00000240423.9 NCAPH
Information
- Transcript ID
- ENST00000240423.9
- Genome
- hg19
- Position
- chr2:97,001,504-97,042,829
- Strand
- +
- CDS length
- 2,226
- Amino acid length
- 742
- Gene symbol
- NCAPH
- Gene type
- protein-coding
- Gene description
- non-SMC condensin I complex subunit H
- Gene Entrez Gene ID
- 23397
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
Exon
| Exon number | Start | Stop |
|---|---|---|
| 1 | 97,001,504 | 97,001,586 |
| 2 | 97,007,380 | 97,007,632 |
| 3 | 97,007,788 | 97,007,878 |
| 4 | 97,008,494 | 97,008,586 |
| 5 | 97,008,904 | 97,009,042 |
| 6 | 97,009,843 | 97,009,967 |
| 7 | 97,017,569 | 97,017,758 |
| 8 | 97,019,044 | 97,019,135 |
| 9 | 97,019,921 | 97,020,126 |
| 10 | 97,024,783 | 97,024,931 |
| 11 | 97,025,881 | 97,025,987 |
| 12 | 97,026,326 | 97,026,448 |
| 13 | 97,030,219 | 97,030,329 |
| 14 | 97,031,614 | 97,031,796 |
| 15 | 97,032,995 | 97,033,111 |
| 16 | 97,034,710 | 97,034,801 |
| 17 | 97,035,163 | 97,035,238 |
| 18 | 97,039,030 | 97,042,829 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 97,001,568 | 97,001,586 |
| 2 | CDS | 97,007,380 | 97,007,632 |
| 3 | CDS | 97,007,788 | 97,007,878 |
| 4 | CDS | 97,008,494 | 97,008,586 |
| 5 | CDS | 97,008,904 | 97,009,042 |
| 6 | CDS | 97,009,843 | 97,009,967 |
| 7 | CDS | 97,017,569 | 97,017,758 |
| 8 | CDS | 97,019,044 | 97,019,135 |
| 9 | CDS | 97,019,921 | 97,020,126 |
| 10 | CDS | 97,024,783 | 97,024,931 |
| 11 | CDS | 97,025,881 | 97,025,987 |
| 12 | CDS | 97,026,326 | 97,026,448 |
| 13 | CDS | 97,030,219 | 97,030,329 |
| 14 | CDS | 97,031,614 | 97,031,796 |
| 15 | CDS | 97,032,995 | 97,033,111 |
| 16 | CDS | 97,034,710 | 97,034,801 |
| 17 | CDS | 97,035,163 | 97,035,238 |
| 18 | CDS | 97,039,030 | 97,039,089 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr2 | 96,335,766 | 96,377,091 | Link |
CDS sequence
ATGGGACCTCCCGGCCCAGCACTGCCAGCCACAATGAATAACTCTTCTTCAGAGACGCGAGGACACCCCCACAGTGCCTCCTCTCCTTCAGAGCGTGTGTTCCCGATGCCCCTGCCCAGGAAGGCGCCTCTCAATATTCCTGGCACCCCAGTCCTCGAAGACTTTCCTCAGAATGACGATGAGAAGGAGCGGCTGCAGCGGAGGCGCTCGAGGGTCTTTGATCTGCAGTTCAGCACTGACTCACCTCGCTTATTGGCCTCCCCCTCCAGCAGGAGTATTGACATTTCAGCTACTATCCCCAAGTTTACAAACACGCAGATTACGGAACATTACTCCACCTGTATCAAACTGTCCACTGAAAATAAAATCACTACCAAGAATGCTTTTGGTTTGCACTTGATTGATTTTATGTCAGAGATTCTTAAACAGAAAGACACCGAACCAACCAACTTTAAAGTGGCTGCGGGTACTCTGGATGCCAGCACCAAGATCTATGCTGTGCGCGTGGATGCCGTCCATGCCGATGTATACAGAGTCCTTGGGGGGCTGGGCAAAGATGCACCGTCTTTGGAAGAAGTAGAAGGCCATGTTGCTGATGGAAGTGCTACTGAAATGGGAACAACCAAAAAGGCTGTAAAGCCAAAGAAGAAGCACTTACACAGAACTATTGAGCAGAACATAAACAACCTCAATGTCTCCGAAGCAGATCGGAAGTGTGAGATTGATCCCATGTTTCAGAAGACAGCAGCCTCATTTGATGAGTGCAGCACAGCAGGGGTGTTTCTGTCCACTCTCCACTGCCAGGACTACAGAAGTGAACTGCTGTTTCCCTCTGATGTCCAGACTCTCTCCACGGGAGAACCTCTCGAGTTGCCAGAGTTAGGTTGTGTAGAAATGACAGATTTAAAAGCGCCCTTGCAGCAGTGTGCAGAAGATCGCCAGATCTGCCCTTCCCTGGCCGGGTTCCAGTTTACACAGTGGGACAGTGAAACACATAATGAGTCTGTGTCGGCCCTGGTAGACAAGTTTAAGAAGAATGACCAGGTATTTGACATCAATGCTGAAGTTGACGAGAGTGACTGTGGAGACTTCCCCGATGGGTCCCTGGGGGATGACTTTGATGCCAACGATGAACCTGACCACACCGCAGTTGGGGATCATGAAGAGTTCAGGAGCTGGAAGGAGCCCTGCCAGGTTCAGAGCTGCCAGGAAGAAATGATTTCCCTTGGGGATGGAGACATCAGGACCATGTGCCCCCTTCTGTCTATGAAACCTGGAGAATATTCTTATTTCAGTCCTCGGACCATGTCGATGTGGGCTGGCCCGGATCACTGGCGCTTTAGGCCTCGACGCAAACAAGATGCTCCTTCCCAATCAGAAAACAAAAAGAAGAGTACAAAAAAAGATTTTGAAATTGACTTTGAAGATGATATTGACTTTGATGTATATTTTAGAAAAACAAAGGCTGCTACTATTCTGACCAAGTCCACTTTGGAGAACCAGAATTGGAGAGCTACCACCCTTCCTACAGATTTCAACTACAATGTTGACACTCTGGTCCAGCTTCACCTCAAACCAGGCACCAGGTTACTTAAGATGGCCCAGGGCCATAGGGTAGAGACTGAGCATTATGAAGAAATTGAAGACTATGATTACAACAACCCTAACGACACCTCCAACTTTTGCCCTGGATTACAGGCTGCTGACAGTGATGATGAAGATTTGGATGACTTATTTGTGGGACCTGTTGGGAACTCTGACCTCTCACCTTATCCTTGCCATCCACCTAAGACAGCACAACAGAATGGTGACACTCCAGAAGCCCAAGGATTAGACATCACAACATATGGGGAGTCAAACTTGGTAGCTGAGCCTCAGAAGGTAAATAAAATTGAAATTCACTATGCCAAGACTGCCAAAAAGATGGACATGAAGAAACTGAAGCAGAGCATGTGGAGTCTGCTGACAGCGCTCTCCGGAAAGGAGGCAGATGCAGAGGCAAACCACAGGGAAGCTGGAAAAGAAGCGGCCCTGGCAGAAGTGGCTGACGAGAAGATGCTTAGCGGGCTCACGAAGGACCTGCAGAGGAGCCTGCCCCCTGTCATGGCTCAGAACCTCTCCATACCTCTGGCTTTTGCCTGTCTCCTACATTTAGCCAATGAAAAGAATCTAAAACTGGAAGGAACAGAGGACCTCTCTGATGTTCTTGTGAGGCAAGGAGATTGA
Amino sequence
MGPPGPALPATMNNSSSETRGHPHSASSPSERVFPMPLPRKAPLNIPGTPVLEDFPQNDDEKERLQRRRSRVFDLQFSTDSPRLLASPSSRSIDISATIPKFTNTQITEHYSTCIKLSTENKITTKNAFGLHLIDFMSEILKQKDTEPTNFKVAAGTLDASTKIYAVRVDAVHADVYRVLGGLGKDAPSLEEVEGHVADGSATEMGTTKKAVKPKKKHLHRTIEQNINNLNVSEADRKCEIDPMFQKTAASFDECSTAGVFLSTLHCQDYRSELLFPSDVQTLSTGEPLELPELGCVEMTDLKAPLQQCAEDRQICPSLAGFQFTQWDSETHNESVSALVDKFKKNDQVFDINAEVDESDCGDFPDGSLGDDFDANDEPDHTAVGDHEEFRSWKEPCQVQSCQEEMISLGDGDIRTMCPLLSMKPGEYSYFSPRTMSMWAGPDHWRFRPRRKQDAPSQSENKKKSTKKDFEIDFEDDIDFDVYFRKTKAATILTKSTLENQNWRATTLPTDFNYNVDTLVQLHLKPGTRLLKMAQGHRVETEHYEEIEDYDYNNPNDTSNFCPGLQAADSDDEDLDDLFVGPVGNSDLSPYPCHPPKTAQQNGDTPEAQGLDITTYGESNLVAEPQKVNKIEIHYAKTAKKMDMKKLKQSMWSLLTALSGKEADAEANHREAGKEAALAEVADEKMLSGLTKDLQRSLPPVMAQNLSIPLAFACLLHLANEKNLKLEGTEDLSDVLVRQGD*