Linked Data
dbSNP Id:
rs1161560614
gnomAD v3:
12-45852774-G-A
gnomAD v4:
12-45852774-G-A
COSMIC:
COSM268370
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.45852774G>A , CM000674.2:g.45852774G>A | GRCh38 |
| NC_000012.11:g.46246557G>A , CM000674.1:g.46246557G>A | GRCh37 |
| NC_000012.10:g.44532824G>A | NCBI36 |
| NG_052800.1:g.128110G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000422737.7:c.4651G>A | ENSP00000415650.3:p.Ala1551Thr | |
| ENST00000457135.2:c.860G>A | ||
| ENST00000334344.11:c.4651G>A MANE Select | ENSP00000335044.6:p.Ala1551Thr | |
| ENST00000422737.6:c.4572G>A | ||
| ENST00000334344.10:c.4651G>A | ENSP00000335044.6:p.Ala1551Thr | |
| ENST00000422737.5:c.4204G>A | ENSP00000415650.1:p.Ala1402Thr | |
| ENST00000444670.5:c.3481G>A | ENSP00000397307.1:p.Ala1161Thr | |
| ENST00000457135.1:c.475G>A | ENSP00000388357.1:p.Ala159Thr | |
| ENST00000479608.5:n.3942G>A | ||
| NM_152641.2:c.4651G>A | NP_689854.2:p.Ala1551Thr | |
| XM_006719272.2:c.4651G>A | XP_006719335.1:p.Ala1551Thr | |
| XM_011538025.1:c.3019G>A | XP_011536327.1:p.Ala1007Thr | |
| XR_944505.1:n.4799G>A | ||
| NM_001347839.1:c.4651G>A | NP_001334768.1:p.Ala1551Thr | |
| NM_152641.3:c.4651G>A | NP_689854.2:p.Ala1551Thr | |
| XM_006719272.4:c.4651G>A | XP_006719335.1:p.Ala1551Thr | |
| XR_944505.3:n.4782G>A | ||
| NM_152641.4:c.4651G>A MANE Select | NP_689854.2:p.Ala1551Thr | |
| NM_001347839.2:c.4651G>A | NP_001334768.1:p.Ala1551Thr |