Linked Data
ClinVar Variation Id:
2720219
ClinVar RCV Id:
RCV003537873
dbSNP Id:
rs1787407031
COSMIC:
COSM28931
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.55191782G>A , CM000669.2:g.55191782G>A | GRCh38 |
| NC_000007.13:g.55259475G>A , CM000669.1:g.55259475G>A | GRCh37 |
| NC_000007.12:g.55226969G>A | NCBI36 |
| NG_007726.3:g.177751G>A , LRG_304:g.177751G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450046.2:c.2374G>A | ENSP00000413354.2:p.Val792Met | |
| ENST00000700145.1:c.882G>A | ||
| ENST00000275493.7:c.2533G>A MANE Select | ENSP00000275493.2:p.Val845Met | |
| ENST00000275493.6:c.2533G>A | ENSP00000275493.2:p.Val845Met | |
| ENST00000442591.5:c.*28+18854G>A | ENSP00000410031.1:n.*28+18854G>A | |
| ENST00000454757.6:c.2398G>A | ENSP00000395243.3:p.Val800Met | |
| ENST00000455089.5:c.2398G>A | ENSP00000415559.1:p.Val800Met | |
| NM_005228.3:c.2533G>A , LRG_304t1:c.2533G>A | NP_005219.2:p.Val845Met | |
| NM_001346897.1:c.2398G>A | NP_001333826.1:p.Val800Met | |
| NM_001346898.1:c.2533G>A | NP_001333827.1:p.Val845Met | |
| NM_001346899.1:c.2398G>A | NP_001333828.1:p.Val800Met | |
| NM_001346900.1:c.2374G>A | NP_001333829.1:p.Val792Met | |
| NM_001346941.1:c.1732G>A | NP_001333870.1:p.Val578Met | |
| NM_005228.4:c.2533G>A | NP_005219.2:p.Val845Met | |
| NM_005228.5:c.2533G>A MANE Select | NP_005219.2:p.Val845Met | |
| NM_001346897.2:c.2398G>A | NP_001333826.1:p.Val800Met | |
| NM_001346898.2:c.2533G>A | NP_001333827.1:p.Val845Met | |
| NM_001346900.2:c.2374G>A | NP_001333829.1:p.Val792Met | |
| NM_001346941.2:c.1732G>A | NP_001333870.1:p.Val578Met | |
| NM_001346899.2:c.2398G>A | NP_001333828.1:p.Val800Met |