Linked Data
ClinVar Variation Id:
283991
dbSNP Id:
rs777323132
ExAC:
15:42691814 C / T
gnomAD v2:
15-42691814-C-T
gnomAD v3:
15-42399616-C-T
gnomAD v4:
15-42399616-C-T
MyVariant Identifiers:
chr15:g.42691814C>T (hg19)
chr15:g.42691814_42691815delinsTG (hg19)
chr15:g.42399616C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42399616C>T , CM000677.2:g.42399616C>T | GRCh38 |
| NC_000015.9:g.42691814C>T , CM000677.1:g.42691814C>T | GRCh37 |
| NC_000015.8:g.40479106C>T | NCBI36 |
| NG_008660.1:g.56514C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.1174C>T | ENSP00000183936.4:p.Arg392Trp | |
| ENST00000357568.8:c.1318C>T | ENSP00000350181.3:p.Arg440Trp | |
| ENST00000397163.8:c.1318C>T MANE Select | ENSP00000380349.3:p.Arg440Trp | |
| ENST00000466369.5:n.1827C>T | ||
| ENST00000483208.5:n.1549C>T | ||
| ENST00000495723.1:n.1549C>T | ||
| ENST00000549793.5:n.1549C>T | ||
| ENST00000638141.2:n.1189C>T | ||
| ENST00000673658.1:n.302C>T | ||
| ENST00000673705.1:c.273C>T | ENSP00000501021.1:n.273C>T | |
| ENST00000318023.11:c.1174C>T | ENSP00000326281.8:p.Arg392Trp | |
| ENST00000349748.7:c.1174C>T | ENSP00000183936.4:p.Arg392Trp | |
| ENST00000357568.7:c.1318C>T | ENSP00000350181.3:p.Arg440Trp | |
| ENST00000397163.7:c.1318C>T | ENSP00000380349.3:p.Arg440Trp | |
| NM_000070.2:c.1318C>T | NP_000061.1:p.Arg440Trp | |
| NM_024344.1:c.1318C>T | NP_077320.1:p.Arg440Trp | |
| NM_173087.1:c.1174C>T | NP_775110.1:p.Arg392Trp | |
| NM_000070.3:c.1318C>T MANE Select | NP_000061.1:p.Arg440Trp | |
| NM_024344.2:c.1318C>T | NP_077320.1:p.Arg440Trp | |
| NM_173087.2:c.1174C>T | NP_775110.1:p.Arg392Trp |