Linked Data
ClinVar Variation Id:
142636
dbSNP Id:
rs587782603
COSMIC:
COSM36365
PubMed:
PMID:23335809
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87952118G>T , CM000672.2:g.87952118G>T | GRCh38 |
| NC_000010.10:g.89711875G>T , CM000672.1:g.89711875G>T | GRCh37 |
| NC_000010.9:g.89701855G>T | NCBI36 |
| NG_007466.2:g.93680G>T , LRG_311:g.93680G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.493G>T | ENSP00000514759.2:p.Gly165Ter | |
| ENST00000710265.1:c.493G>T | ENSP00000518161.1:p.Gly165Ter | |
| ENST00000472832.3:c.493G>T | ENSP00000483066.2:p.Gly165Ter | |
| ENST00000688158.2:n.1228G>T | ||
| ENST00000688922.2:c.*323G>T | ENSP00000508742.2:n.*323G>T | |
| ENST00000700021.1:c.448G>T | ENSP00000514757.1:p.Gly150Ter | |
| ENST00000700022.1:c.493-5735G>T | ENSP00000514758.1:n.493-5735G>T | |
| ENST00000700023.1:n.1651G>T | ||
| ENST00000700024.1:n.1885G>T | ||
| ENST00000700025.1:n.1262G>T | ||
| ENST00000700029.1:c.327G>T | ||
| ENST00000706954.1:c.493G>T | ENSP00000516674.1:p.Gly165Ter | |
| ENST00000706955.1:c.*528G>T | ENSP00000516675.1:n.*528G>T | |
| ENST00000686459.1:c.*79G>T | ENSP00000508909.1:n.*79G>T | |
| ENST00000688158.1:c.*604G>T | ENSP00000509254.1:n.*604G>T | |
| ENST00000688308.1:c.493G>T | ENSP00000508752.1:p.Gly165Ter | |
| ENST00000688922.1:c.414G>T | ||
| ENST00000693560.1:c.1012G>T | ENSP00000509861.1:p.Gly338Ter | |
| ENST00000371953.8:c.493G>T MANE Select | ENSP00000361021.3:p.Gly165Ter | |
| ENST00000371953.7:c.493G>T | ENSP00000361021.3:p.Gly165Ter | |
| NM_000314.5:c.493G>T | NP_000305.3:p.Gly165Ter | |
| NM_000314.6:c.493G>T | NP_000305.3:p.Gly165Ter | |
| NM_001304717.2:c.1012G>T | NP_001291646.2:p.Gly338Ter | |
| NM_001304718.1:c.-99G>T | NP_001291647.1:n.-99G>T | |
| XM_006717926.2:c.448G>T | XP_006717989.1:p.Gly150Ter | |
| XM_011539981.1:c.493G>T | XP_011538283.1:p.Gly165Ter | |
| XM_011539982.1:c.397G>T | XP_011538284.1:p.Gly133Ter | |
| XR_945789.1:n.1364G>T | ||
| XR_945790.1:n.1481G>T | ||
| XR_945791.1:n.1205-5735G>T | ||
| NM_000314.7:c.493G>T | NP_000305.3:p.Gly165Ter | |
| NM_001304717.5:c.1012G>T | NP_001291646.4:p.Gly338Ter | |
| NM_001304718.2:c.-99G>T | NP_001291647.1:n.-99G>T | |
| NM_000314.8:c.493G>T MANE Select | NP_000305.3:p.Gly165Ter |