Linked Data
ClinVar Variation Id:
1059075
ClinVar RCV Id:
RCV001368289
dbSNP Id:
rs764650219
COSMIC:
COSM1126592
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.100407301G>T , CM000685.2:g.100407301G>T | GRCh38 |
| NC_000023.10:g.99662299G>T , CM000685.1:g.99662299G>T | GRCh37 |
| NC_000023.9:g.99548955G>T | NCBI36 |
| NG_021319.1:g.7973C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000255531.8:c.1297C>A | ENSP00000255531.7:p.Leu433Met | |
| ENST00000373034.8:c.1297C>A MANE Select | ENSP00000362125.4:p.Leu433Met | |
| ENST00000420881.6:c.1297C>A | ENSP00000400327.2:p.Leu433Met | |
| NM_001105243.1:c.1297C>A | NP_001098713.1:p.Leu433Met | |
| NM_001184880.1:c.1297C>A | NP_001171809.1:p.Leu433Met | |
| NM_020766.2:c.1297C>A | NP_065817.2:p.Leu433Met | |
| XM_011530997.1:c.1297C>A | XP_011529299.1:p.Leu433Met | |
| XM_011530997.2:c.1297C>A | XP_011529299.1:p.Leu433Met | |
| NM_001105243.2:c.1297C>A | NP_001098713.1:p.Leu433Met | |
| NM_001184880.2:c.1297C>A MANE Select | NP_001171809.1:p.Leu433Met | |
| NM_020766.3:c.1297C>A | NP_065817.2:p.Leu433Met |