Linked Data
ClinVar Variation Id:
13972
ClinVar RCV Id:
RCV000015006
RCV000037932
RCV000418680
RCV000423919
RCV000426107
RCV000433779
RCV000437006
RCV000426339
RCV000435875
RCV000443065
RCV000443882
RCV001238853
RCV000442759
dbSNP Id:
rs121913338
COSMIC:
COSM467
CIViC:
CA123657
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140753354T>C , CM000669.2:g.140753354T>C | GRCh38 |
| NC_000007.13:g.140453154T>C , CM000669.1:g.140453154T>C | GRCh37 |
| NC_000007.12:g.140099623T>C | NCBI36 |
| NG_007873.3:g.176411A>G , LRG_299:g.176411A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.1781A>G MANE Select | ENSP00000493543.1:p.Asp594Gly | |
| ENST00000288602.11:c.1901A>G | ENSP00000288602.7:p.Asp634Gly | |
| ENST00000479537.6:c.451A>G | ||
| ENST00000496384.7:c.1781A>G | ENSP00000419060.2:p.Asp594Gly | |
| ENST00000497784.2:c.*1231A>G | ENSP00000420119.2:n.*1231A>G | |
| ENST00000642228.1:c.*859A>G | ENSP00000493678.1:n.*859A>G | |
| ENST00000642875.1:n.1259-3936A>G | ||
| ENST00000644120.1:n.2171A>G | ||
| ENST00000644650.1:c.877A>G | ||
| ENST00000644905.1:n.2663A>G | ||
| ENST00000644969.2:c.1901A>G MANE Plus Clinical | ENSP00000496776.1:p.Asp634Gly | |
| ENST00000646730.1:c.*357A>G | ENSP00000494784.1:n.*357A>G | |
| ENST00000646891.1:c.1781A>G | ENSP00000493543.1:p.Asp594Gly | |
| ENST00000647434.1:c.738-3936A>G | ENSP00000495132.1:n.738-3936A>G | |
| ENST00000288602.10:c.1781A>G | ENSP00000288602.6:p.Asp594Gly | |
| ENST00000479537.5:c.65A>G | ENSP00000418033.1:p.Asp22Gly | |
| ENST00000496384.6:c.604A>G | ||
| ENST00000497784.1:c.1816A>G | ENSP00000420119.1:n.1816A>G | |
| NM_004333.4:c.1781A>G , LRG_299t1:c.1781A>G | NP_004324.2:p.Asp594Gly | |
| XM_005250045.1:c.1781A>G | XP_005250102.1:p.Asp594Gly | |
| XM_005250046.1:c.1781A>G | XP_005250103.1:p.Asp594Gly | |
| XM_011516529.1:c.1781A>G | XP_011514831.1:p.Asp594Gly | |
| XM_011516530.1:c.1695-3936A>G | XP_011514832.1:n.1695-3936A>G | |
| XR_242190.1:n.1789A>G | ||
| XR_927520.1:n.1789A>G | ||
| XR_927521.1:n.1789A>G | ||
| XR_927522.1:n.1703-3936A>G | ||
| XR_927523.1:n.1703-3936A>G | ||
| NM_001354609.1:c.1781A>G | NP_001341538.1:p.Asp594Gly | |
| NM_004333.5:c.1781A>G | NP_004324.2:p.Asp594Gly | |
| NR_148928.1:n.2879A>G | ||
| XM_017012558.1:c.1901A>G | XP_016868047.1:p.Asp634Gly | |
| XM_017012559.1:c.1901A>G | XP_016868048.1:p.Asp634Gly | |
| XR_001744857.1:n.1909A>G | ||
| XR_001744858.1:n.1823-3936A>G | ||
| NM_001354609.2:c.1781A>G | NP_001341538.1:p.Asp594Gly | |
| NM_001374244.1:c.1901A>G | NP_001361173.1:p.Asp634Gly | |
| NM_001374258.1:c.1901A>G MANE Plus Clinical | NP_001361187.1:p.Asp634Gly | |
| NM_004333.6:c.1781A>G MANE Select | NP_004324.2:p.Asp594Gly | |
| NM_001378467.1:c.1790A>G | NP_001365396.1:p.Asp597Gly | |
| NM_001378468.1:c.1781A>G | NP_001365397.1:p.Asp594Gly | |
| NM_001378469.1:c.1715A>G | NP_001365398.1:p.Asp572Gly | |
| NM_001378470.1:c.1679A>G | NP_001365399.1:p.Asp560Gly | |
| NM_001378471.1:c.1670A>G | NP_001365400.1:p.Asp557Gly | |
| NM_001378472.1:c.1625A>G | NP_001365401.1:p.Asp542Gly | |
| NM_001378473.1:c.1625A>G | NP_001365402.1:p.Asp542Gly | |
| NM_001378474.1:c.1781A>G | NP_001365403.1:p.Asp594Gly | |
| NM_001378475.1:c.1517A>G | NP_001365404.1:p.Asp506Gly |