Linked Data
ClinVar Variation Id:
92820
dbSNP Id:
rs398123321
COSMIC:
COSM5121
ERepo:
CA000401/MONDO:0017623/003
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87933090T>C , CM000672.2:g.87933090T>C | GRCh38 |
| NC_000010.10:g.89692847T>C , CM000672.1:g.89692847T>C | GRCh37 |
| NC_000010.9:g.89682827T>C | NCBI36 |
| NG_007466.2:g.74652T>C , LRG_311:g.74652T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.331T>C | ENSP00000514759.2:p.Trp111Arg | |
| ENST00000710265.1:c.331T>C | ENSP00000518161.1:p.Trp111Arg | |
| ENST00000472832.3:c.331T>C | ENSP00000483066.2:p.Trp111Arg | |
| ENST00000688158.2:n.1066T>C | ||
| ENST00000688922.2:c.*161T>C | ENSP00000508742.2:n.*161T>C | |
| ENST00000700021.1:c.286T>C | ENSP00000514757.1:p.Trp96Arg | |
| ENST00000700022.1:c.331T>C | ENSP00000514758.1:p.Trp111Arg | |
| ENST00000700029.1:c.165T>C | ||
| ENST00000706954.1:c.331T>C | ENSP00000516674.1:p.Trp111Arg | |
| ENST00000706955.1:c.*366T>C | ENSP00000516675.1:n.*366T>C | |
| ENST00000686459.1:c.331T>C | ENSP00000508909.1:p.Trp111Arg | |
| ENST00000688158.1:c.*442T>C | ENSP00000509254.1:n.*442T>C | |
| ENST00000688308.1:c.331T>C | ENSP00000508752.1:p.Trp111Arg | |
| ENST00000688922.1:c.252T>C | ||
| ENST00000693560.1:c.850T>C | ENSP00000509861.1:p.Trp284Arg | |
| ENST00000371953.8:c.331T>C MANE Select | ENSP00000361021.3:p.Trp111Arg | |
| ENST00000371953.7:c.331T>C | ENSP00000361021.3:p.Trp111Arg | |
| ENST00000498703.1:n.157T>C | ||
| ENST00000610634.1:c.229T>C | ENSP00000477517.1:p.Trp77Arg | |
| NM_000314.5:c.331T>C | NP_000305.3:p.Trp111Arg | |
| NM_000314.6:c.331T>C | NP_000305.3:p.Trp111Arg | |
| NM_001304717.2:c.850T>C | NP_001291646.2:p.Trp284Arg | |
| NM_001304718.1:c.-420T>C | NP_001291647.1:n.-420T>C | |
| XM_006717926.2:c.286T>C | XP_006717989.1:p.Trp96Arg | |
| XM_011539981.1:c.331T>C | XP_011538283.1:p.Trp111Arg | |
| XM_011539982.1:c.235T>C | XP_011538284.1:p.Trp79Arg | |
| XR_945789.1:n.1043T>C | ||
| XR_945790.1:n.1043T>C | ||
| XR_945791.1:n.1043T>C | ||
| NM_000314.7:c.331T>C | NP_000305.3:p.Trp111Arg | |
| NM_001304717.5:c.850T>C | NP_001291646.4:p.Trp284Arg | |
| NM_001304718.2:c.-420T>C | NP_001291647.1:n.-420T>C | |
| NM_000314.8:c.331T>C MANE Select | NP_000305.3:p.Trp111Arg |