Linked Data
ClinVar Variation Id:
468831
dbSNP Id:
rs148698633
ExAC:
11:22279254 C / T
gnomAD v2:
11-22279254-C-T
gnomAD v3:
11-22257708-C-T
gnomAD v4:
11-22257708-C-T
COSMIC:
COSM1581836
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22257708C>T , CM000673.2:g.22257708C>T | GRCh38 |
| NC_000011.9:g.22279254C>T , CM000673.1:g.22279254C>T | GRCh37 |
| NC_000011.8:g.22235830C>T | NCBI36 |
| NG_015844.1:g.69533C>T , LRG_868:g.69533C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682266.1:c.911C>T | ENSP00000507766.1:p.Thr304Met | |
| ENST00000682341.1:c.1319C>T | ENSP00000508251.1:p.Thr440Met | |
| ENST00000683197.1:c.1319C>T | ENSP00000507641.1:p.Thr440Met | |
| ENST00000683411.1:c.911C>T | ENSP00000508397.1:p.Thr304Met | |
| ENST00000683437.1:c.911C>T | ENSP00000508408.1:p.Thr304Met | |
| ENST00000683613.1:n.2355C>T | ||
| ENST00000684663.1:c.1316C>T | ENSP00000508009.1:p.Thr439Met | |
| ENST00000324559.9:c.1361C>T MANE Select | ENSP00000315371.9:p.Thr454Met | |
| ENST00000648804.1:n.1696C>T | ||
| ENST00000324559.8:c.1361C>T | ENSP00000315371.8:p.Thr454Met | |
| NM_001142649.1:c.1358C>T | NP_001136121.1:p.Thr453Met | |
| NM_213599.2:c.1361C>T , LRG_868t1:c.1361C>T | NP_998764.1:p.Thr454Met | |
| XM_005252820.2:c.1319C>T | XP_005252877.2:p.Thr440Met | |
| XM_005252821.2:c.1316C>T | XP_005252878.2:p.Thr439Met | |
| XM_005252822.3:c.1283C>T | XP_005252879.1:p.Thr428Met | |
| XM_005252823.3:c.1280C>T | XP_005252880.1:p.Thr427Met | |
| XM_011519949.1:c.1268C>T | XP_011518251.1:p.Thr423Met | |
| XM_005252820.3:c.1319C>T | XP_005252877.2:p.Thr440Met | |
| XM_005252821.3:c.1316C>T | XP_005252878.2:p.Thr439Met | |
| XM_005252822.4:c.1283C>T | XP_005252879.1:p.Thr428Met | |
| XM_011519949.2:c.1268C>T | XP_011518251.1:p.Thr423Met | |
| NM_001142649.2:c.1358C>T | NP_001136121.1:p.Thr453Met | |
| NM_213599.3:c.1361C>T MANE Select | NP_998764.1:p.Thr454Met |