ENST00000240423.9 NCAPH
Information
- Transcript ID
- ENST00000240423.9
- Genome
- hg38
- Position
- chr2:96,335,766-96,377,091
- 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
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Category | : |
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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 | 96,335,766 | 96,335,848 |
2 | 96,341,642 | 96,341,894 |
3 | 96,342,050 | 96,342,140 |
4 | 96,342,756 | 96,342,848 |
5 | 96,343,166 | 96,343,304 |
6 | 96,344,105 | 96,344,229 |
7 | 96,351,831 | 96,352,020 |
8 | 96,353,306 | 96,353,397 |
9 | 96,354,183 | 96,354,388 |
10 | 96,359,045 | 96,359,193 |
11 | 96,360,143 | 96,360,249 |
12 | 96,360,588 | 96,360,710 |
13 | 96,364,481 | 96,364,591 |
14 | 96,365,876 | 96,366,058 |
15 | 96,367,257 | 96,367,373 |
16 | 96,368,972 | 96,369,063 |
17 | 96,369,425 | 96,369,500 |
18 | 96,373,292 | 96,377,091 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 96,335,830 | 96,335,848 |
2 | CDS | 96,341,642 | 96,341,894 |
3 | CDS | 96,342,050 | 96,342,140 |
4 | CDS | 96,342,756 | 96,342,848 |
5 | CDS | 96,343,166 | 96,343,304 |
6 | CDS | 96,344,105 | 96,344,229 |
7 | CDS | 96,351,831 | 96,352,020 |
8 | CDS | 96,353,306 | 96,353,397 |
9 | CDS | 96,354,183 | 96,354,388 |
10 | CDS | 96,359,045 | 96,359,193 |
11 | CDS | 96,360,143 | 96,360,249 |
12 | CDS | 96,360,588 | 96,360,710 |
13 | CDS | 96,364,481 | 96,364,591 |
14 | CDS | 96,365,876 | 96,366,058 |
15 | CDS | 96,367,257 | 96,367,373 |
16 | CDS | 96,368,972 | 96,369,063 |
17 | CDS | 96,369,425 | 96,369,500 |
18 | CDS | 96,373,292 | 96,373,351 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr2 | 97,001,504 | 97,042,829 | Link |
CDS sequence
ATGGGACCTCCCGGCCCAGCACTGCCAGCCACAATGAATAACTCTTCTTCAGAGACGCGAGGACACCCCCACAGTGCCTCCTCTCCTTCAGAGCGTGTGTTCCCGATGCCCCTGCCCAGGAAGGCGCCTCTCAATATTCCTGGCACCCCAGTCCTCGAAGACTTTCCTCAGAATGACGATGAGAAGGAGCGGCTGCAGCGGAGGCGCTCGAGGGTCTTTGATCTGCAGTTCAGCACTGACTCACCTCGCTTATTGGCCTCCCCCTCCAGCAGGAGTATTGACATTTCAGCTACTATCCCCAAGTTTACAAACACGCAGATTACGGAACATTACTCCACCTGTATCAAACTGTCCACTGAAAATAAAATCACTACCAAGAATGCTTTTGGTTTGCACTTGATTGATTTTATGTCAGAGATTCTTAAACAGAAAGACACCGAACCAACCAACTTTAAAGTGGCTGCGGGTACTCTGGATGCCAGCACCAAGATCTATGCTGTGCGCGTGGATGCCGTCCATGCCGATGTATACAGAGTCCTTGGGGGGCTGGGCAAAGATGCACCGTCTTTGGAAGAAGTAGAAGGCCATGTTGCTGATGGAAGTGCTACTGAAATGGGAACAACCAAAAAGGCTGTAAAGCCAAAGAAGAAGCACTTACACAGAACTATTGAGCAGAACATAAACAACCTCAATGTCTCCGAAGCAGATCGGAAGTGTGAGATTGATCCCATGTTTCAGAAGACAGCAGCCTCATTTGATGAGTGCAGCACAGCAGGGGTGTTTCTGTCCACTCTCCACTGCCAGGACTACAGAAGTGAACTGCTGTTTCCCTCTGATGTCCAGACTCTCTCCACGGGAGAACCTCTCGAGTTGCCAGAGTTAGGTTGTGTAGAAATGACAGATTTAAAAGCGCCCTTGCAGCAGTGTGCAGAAGATCGCCAGATCTGCCCTTCCCTGGCCGGGTTCCAGTTTACACAGTGGGACAGTGAAACACATAATGAGTCTGTGTCGGCCCTGGTAGACAAGTTTAAGAAGAATGACCAGGTATTTGACATCAATGCTGAAGTTGACGAGAGTGACTGTGGAGACTTCCCCGATGGGTCCCTGGGGGATGACTTTGATGCCAACGATGAACCTGACCACACCGCAGTTGGGGATCATGAAGAGTTCAGGAGCTGGAAGGAGCCCTGCCAGGTTCAGAGCTGCCAGGAAGAAATGATTTCCCTTGGGGATGGAGACATCAGGACCATGTGCCCCCTTCTGTCTATGAAACCTGGAGAATATTCTTATTTCAGTCCTCGGACCATGTCGATGTGGGCTGGCCCGGATCACTGGCGCTTTAGGCCTCGACGCAAACAAGATGCTCCTTCCCAATCAGAAAACAAAAAGAAGAGTACAAAAAAAGATTTTGAAATTGACTTTGAAGATGATATTGACTTTGATGTATATTTTAGAAAAACAAAGGCTGCTACTATTCTGACCAAGTCCACTTTGGAGAACCAGAATTGGAGAGCTACCACCCTTCCTACAGATTTCAACTACAATGTTGACACTCTGGTCCAGCTTCACCTCAAACCAGGCACCAGGTTACTTAAGATGGCCCAGGGCCATAGGGTAGAGACTGAGCATTATGAAGAAATTGAAGACTATGATTACAACAACCCTAACGACACCTCCAACTTTTGCCCTGGATTACAGGCTGCTGACAGTGATGATGAAGATTTGGATGACTTATTTGTGGGACCTGTTGGGAACTCTGACCTCTCACCTTATCCTTGCCATCCACCTAAGACAGCACAACAGAATGGTGACACTCCAGAAGCCCAAGGATTAGACATCACAACATATGGGGAGTCAAACTTGGTAGCTGAGCCTCAGAAGGTAAATAAAATTGAAATTCACTATGCCAAGACTGCCAAAAAGATGGACATGAAGAAACTGAAGCAGAGCATGTGGAGTCTGCTGACAGCGCTCTCCGGAAAGGAGGCAGATGCAGAGGCAAACCACAGGGAAGCTGGAAAAGAAGCGGCCCTGGCAGAAGTGGCTGACGAGAAGATGCTTAGCGGGCTCACGAAGGACCTGCAGAGGAGCCTGCCCCCTGTCATGGCTCAGAACCTCTCCATACCTCTGGCTTTTGCCTGTCTCCTACATTTAGCCAATGAAAAGAATCTAAAACTGGAAGGAACAGAGGACCTCTCTGATGTTCTTGTGAGGCAAGGAGATTGA
Amino sequence
MGPPGPALPATMNNSSSETRGHPHSASSPSERVFPMPLPRKAPLNIPGTPVLEDFPQNDDEKERLQRRRSRVFDLQFSTDSPRLLASPSSRSIDISATIPKFTNTQITEHYSTCIKLSTENKITTKNAFGLHLIDFMSEILKQKDTEPTNFKVAAGTLDASTKIYAVRVDAVHADVYRVLGGLGKDAPSLEEVEGHVADGSATEMGTTKKAVKPKKKHLHRTIEQNINNLNVSEADRKCEIDPMFQKTAASFDECSTAGVFLSTLHCQDYRSELLFPSDVQTLSTGEPLELPELGCVEMTDLKAPLQQCAEDRQICPSLAGFQFTQWDSETHNESVSALVDKFKKNDQVFDINAEVDESDCGDFPDGSLGDDFDANDEPDHTAVGDHEEFRSWKEPCQVQSCQEEMISLGDGDIRTMCPLLSMKPGEYSYFSPRTMSMWAGPDHWRFRPRRKQDAPSQSENKKKSTKKDFEIDFEDDIDFDVYFRKTKAATILTKSTLENQNWRATTLPTDFNYNVDTLVQLHLKPGTRLLKMAQGHRVETEHYEEIEDYDYNNPNDTSNFCPGLQAADSDDEDLDDLFVGPVGNSDLSPYPCHPPKTAQQNGDTPEAQGLDITTYGESNLVAEPQKVNKIEIHYAKTAKKMDMKKLKQSMWSLLTALSGKEADAEANHREAGKEAALAEVADEKMLSGLTKDLQRSLPPVMAQNLSIPLAFACLLHLANEKNLKLEGTEDLSDVLVRQGD*