Linked Data
ClinVar Variation Id:
280724
dbSNP Id:
rs886041877
COSMIC:
COSM5247
ERepo:
CA10603162/MONDO:0017623/003
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87894025A>C , CM000672.2:g.87894025A>C | GRCh38 |
| NC_000010.10:g.89653782A>C , CM000672.1:g.89653782A>C | GRCh37 |
| NC_000010.9:g.89643762A>C | NCBI36 |
| NG_007466.2:g.35587A>C , LRG_311:g.35587A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.80A>C | ENSP00000514759.2:p.Tyr27Ser | |
| ENST00000710265.1:c.80A>C | ENSP00000518161.1:p.Tyr27Ser | |
| ENST00000472832.3:c.80A>C | ENSP00000483066.2:p.Tyr27Ser | |
| ENST00000688158.2:n.899+13587A>C | ||
| ENST00000688922.2:c.80A>C | ENSP00000508742.2:p.Tyr27Ser | |
| ENST00000700021.1:c.80A>C | ENSP00000514757.1:p.Tyr27Ser | |
| ENST00000700022.1:c.80A>C | ENSP00000514758.1:p.Tyr27Ser | |
| ENST00000706954.1:c.80A>C | ENSP00000516674.1:p.Tyr27Ser | |
| ENST00000706955.1:c.*115A>C | ENSP00000516675.1:n.*115A>C | |
| ENST00000686459.1:c.80A>C | ENSP00000508909.1:p.Tyr27Ser | |
| ENST00000688158.1:c.*275+13587A>C | ENSP00000509254.1:n.*275+13587A>C | |
| ENST00000688308.1:c.80A>C | ENSP00000508752.1:p.Tyr27Ser | |
| ENST00000693560.1:c.599A>C | ENSP00000509861.1:p.Tyr200Ser | |
| ENST00000371953.8:c.80A>C MANE Select | ENSP00000361021.3:p.Tyr27Ser | |
| ENST00000371953.7:c.80A>C | ENSP00000361021.3:p.Tyr27Ser | |
| ENST00000462694.1:n.82A>C | ||
| ENST00000610634.1:c.-23A>C | ENSP00000477517.1:n.-23A>C | |
| NM_000314.5:c.80A>C | NP_000305.3:p.Tyr27Ser | |
| NM_000314.6:c.80A>C | NP_000305.3:p.Tyr27Ser | |
| NM_001304717.2:c.599A>C | NP_001291646.2:p.Tyr200Ser | |
| NM_001304718.1:c.-626A>C | NP_001291647.1:n.-626A>C | |
| XM_006717926.2:c.80A>C | XP_006717989.1:p.Tyr27Ser | |
| XM_011539981.1:c.80A>C | XP_011538283.1:p.Tyr27Ser | |
| XM_011539982.1:c.68+13587A>C | XP_011538284.1:n.68+13587A>C | |
| XR_945789.1:n.792A>C | ||
| XR_945790.1:n.792A>C | ||
| XR_945791.1:n.792A>C | ||
| NM_000314.7:c.80A>C | NP_000305.3:p.Tyr27Ser | |
| NM_001304717.5:c.599A>C | NP_001291646.4:p.Tyr200Ser | |
| NM_001304718.2:c.-626A>C | NP_001291647.1:n.-626A>C | |
| NM_000314.8:c.80A>C MANE Select | NP_000305.3:p.Tyr27Ser |