ENST00000703798.1 NAP1L4
Information
- Transcript ID
- ENST00000703798.1
- Genome
- hg19
- Position
- chr11:2,965,667-3,013,522
- Strand
- -
- CDS length
- 1,164
- Amino acid length
- 388
- Gene symbol
- NAP1L4
- Gene type
- protein-coding
- Gene description
- nucleosome assembly protein 1 like 4
- Gene Entrez Gene ID
- 4676
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 |
---|---|---|
16 | 2,965,667 | 2,966,876 |
15 | 2,970,457 | 2,970,494 |
14 | 2,972,489 | 2,972,545 |
13 | 2,973,010 | 2,973,039 |
12 | 2,975,757 | 2,975,876 |
11 | 2,976,974 | 2,976,996 |
10 | 2,979,629 | 2,979,774 |
9 | 2,981,000 | 2,981,139 |
8 | 2,985,910 | 2,985,981 |
7 | 2,991,033 | 2,991,164 |
6 | 2,992,678 | 2,992,764 |
5 | 2,993,332 | 2,993,509 |
4 | 2,997,254 | 2,997,353 |
3 | 2,999,514 | 2,999,572 |
2 | 3,000,437 | 3,000,467 |
1 | 3,013,484 | 3,013,522 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
15 | CDS | 2,970,489 | 2,970,494 |
14 | CDS | 2,972,489 | 2,972,545 |
13 | CDS | 2,973,010 | 2,973,039 |
12 | CDS | 2,975,757 | 2,975,876 |
11 | CDS | 2,976,974 | 2,976,996 |
10 | CDS | 2,979,629 | 2,979,774 |
9 | CDS | 2,981,000 | 2,981,139 |
8 | CDS | 2,985,910 | 2,985,981 |
7 | CDS | 2,991,033 | 2,991,164 |
6 | CDS | 2,992,678 | 2,992,764 |
5 | CDS | 2,993,332 | 2,993,509 |
4 | CDS | 2,997,254 | 2,997,353 |
3 | CDS | 2,999,514 | 2,999,572 |
2 | CDS | 3,000,437 | 3,000,450 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr11 | 2,944,437 | 2,992,292 | Link |
CDS sequence
ATGGCAGATCACAGTTTTTCAGATGGGGTTCCTTCAGATTCCGTGGAAGCTGCTAAAAATGCAAGTAACACAGAAAAGCTCACAGATCAGGTGATGCAGAATCCTCGAGTTCTGGCAGCTTTACAGGAGCGACTTGACAATGTCCCTCACACCCCTTCCAGCTACATCGAAACGCATGAGGATGTTGTATTTCTTACTCCCTTTTTTAGTTTACCTAAAGCAGTAAAAAGAAGAATTAATGCATTGAAACAACTTCAGGTGAGATGTGCTCACATAGAAGCCAAGTTCTATGAAGAGGTACATGACTTGGAAAGAAAGTATGCAGCGCTATACCAGCCTCTCTTTGACAAGAGAAGAGAATTTATCACCGGCGATGTTGAACCAACAGATGCGGAATCGGAATGGCACAGTGAAAATGAAGAGGAAGAGAAATTGGCTGGAGACATGAAAAGTAAAGTAGTCGTCACAGAAAAAGCAGCGGCAACGGCTGAAGAGCCAGATCCCAAAGGAATTCCAGAGTTCTGGTTTACCATCTTCAGAAATGTGGACATGCTGAGTGAATTAGTCCAGGAATATGATGAACCAATCTTGAAACACCTGCAGGATATTAAAGTGAAATTTTCTGACCCTGGACAGCCTATGTCTTTTGTGTTAGAGTTCCACTTTGAACCCAACGACTACTTTACCAACTCAGTCCTGACAAAAACCTACAAGATGAAATCAGAACCAGATAAGGCTGATCCCTTTTCCTTTGAAGGTCCTGAGATTGTGGACTGTGACGGGTGTACTATTGACTGGAAGAAAGGAAAGAATGTTACTGTCAAAACCATCAAGAAAAAGCAGAAGCATAAGGGTCGAGGCACTGTTAGAACAATTACGAAACAAGTACCCAATGAGTCCTTTTTCAACTTCTTCAATCCATTGAAAGCATCCGGGGATGGAGAATCACTGGATGAAGATTCTGAATTCACATTAGCCTCTGATTTTGAAATTGGACACTTTTTCCGTGAGCGGATAGTCCCGCGGGCTGTGCTGTACTTCACTGGGGAGGCCATAGAAGATGATGACAATTTTGAAGAAGGTGAAGAAGGAGAAGAGGAGGAATTAGAAGGTGACGAGGAGGGAGAAGACGAGGATGATGCGGAAATTAACCCCAAGGTGTAA
Amino sequence
MADHSFSDGVPSDSVEAAKNASNTEKLTDQVMQNPRVLAALQERLDNVPHTPSSYIETHEDVVFLTPFFSLPKAVKRRINALKQLQVRCAHIEAKFYEEVHDLERKYAALYQPLFDKRREFITGDVEPTDAESEWHSENEEEEKLAGDMKSKVVVTEKAAATAEEPDPKGIPEFWFTIFRNVDMLSELVQEYDEPILKHLQDIKVKFSDPGQPMSFVLEFHFEPNDYFTNSVLTKTYKMKSEPDKADPFSFEGPEIVDCDGCTIDWKKGKNVTVKTIKKKQKHKGRGTVRTITKQVPNESFFNFFNPLKASGDGESLDEDSEFTLASDFEIGHFFRERIVPRAVLYFTGEAIEDDDNFEEGEEGEEEELEGDEEGEDEDDAEINPKV*