Linked Data
ClinVar Variation Id:
92822
dbSNP Id:
rs121909241
COSMIC:
COSM5123
ERepo:
CA000444/MONDO:0017623/003
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87933154G>A , CM000672.2:g.87933154G>A | GRCh38 |
| NC_000010.10:g.89692911G>A , CM000672.1:g.89692911G>A | GRCh37 |
| NC_000010.9:g.89682891G>A | NCBI36 |
| NG_007466.2:g.74716G>A , LRG_311:g.74716G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.395G>A | ENSP00000514759.2:p.Gly132Asp | |
| ENST00000710265.1:c.395G>A | ENSP00000518161.1:p.Gly132Asp | |
| ENST00000472832.3:c.395G>A | ENSP00000483066.2:p.Gly132Asp | |
| ENST00000688158.2:n.1130G>A | ||
| ENST00000688922.2:c.*225G>A | ENSP00000508742.2:n.*225G>A | |
| ENST00000700021.1:c.350G>A | ENSP00000514757.1:p.Gly117Asp | |
| ENST00000700022.1:c.395G>A | ENSP00000514758.1:p.Gly132Asp | |
| ENST00000700029.1:c.229G>A | ||
| ENST00000706954.1:c.395G>A | ENSP00000516674.1:p.Gly132Asp | |
| ENST00000706955.1:c.*430G>A | ENSP00000516675.1:n.*430G>A | |
| ENST00000686459.1:c.395G>A | ENSP00000508909.1:p.Gly132Asp | |
| ENST00000688158.1:c.*506G>A | ENSP00000509254.1:n.*506G>A | |
| ENST00000688308.1:c.395G>A | ENSP00000508752.1:p.Gly132Asp | |
| ENST00000688922.1:c.316G>A | ||
| ENST00000693560.1:c.914G>A | ENSP00000509861.1:p.Gly305Asp | |
| ENST00000371953.8:c.395G>A MANE Select | ENSP00000361021.3:p.Gly132Asp | |
| ENST00000371953.7:c.395G>A | ENSP00000361021.3:p.Gly132Asp | |
| ENST00000498703.1:n.221G>A | ||
| ENST00000610634.1:c.293G>A | ENSP00000477517.1:p.Gly98Asp | |
| NM_000314.5:c.395G>A | NP_000305.3:p.Gly132Asp | |
| NM_000314.6:c.395G>A | NP_000305.3:p.Gly132Asp | |
| NM_001304717.2:c.914G>A | NP_001291646.2:p.Gly305Asp | |
| NM_001304718.1:c.-356G>A | NP_001291647.1:n.-356G>A | |
| XM_006717926.2:c.350G>A | XP_006717989.1:p.Gly117Asp | |
| XM_011539981.1:c.395G>A | XP_011538283.1:p.Gly132Asp | |
| XM_011539982.1:c.299G>A | XP_011538284.1:p.Gly100Asp | |
| XR_945789.1:n.1107G>A | ||
| XR_945790.1:n.1107G>A | ||
| XR_945791.1:n.1107G>A | ||
| NM_000314.7:c.395G>A | NP_000305.3:p.Gly132Asp | |
| NM_001304717.5:c.914G>A | NP_001291646.4:p.Gly305Asp | |
| NM_001304718.2:c.-356G>A | NP_001291647.1:n.-356G>A | |
| NM_000314.8:c.395G>A MANE Select | NP_000305.3:p.Gly132Asp |