Linked Data
ClinVar Variation Id:
83238
ClinVar RCV Id:
RCV000074229
dbSNP Id:
rs79512956
COSMIC:
COSM1567173
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112838104C>A , CM000667.2:g.112838104C>A | GRCh38 |
| NC_000005.9:g.112173801C>A , CM000667.1:g.112173801C>A | GRCh37 |
| NC_000005.8:g.112201700C>A | NCBI36 |
| NG_008481.4:g.150584C>A , LRG_130:g.150584C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.2175C>A | ENSP00000484935.2:n.2175C>A | |
| ENST00000504915.3:c.2564C>A | ENSP00000473355.2:p.Ser855Ter | |
| ENST00000505350.2:c.*2516C>A | ENSP00000481752.1:n.*2516C>A | |
| ENST00000507379.6:c.2456C>A | ENSP00000423224.2:p.Ser819Ter | |
| ENST00000509732.6:c.2510C>A | ENSP00000426541.2:p.Ser837Ter | |
| ENST00000512211.7:c.2510C>A | ENSP00000423828.3:p.Ser837Ter | |
| ENST00000257430.9:c.2510C>A MANE Select | ENSP00000257430.4:p.Ser837Ter | |
| ENST00000257430.8:c.2510C>A | ENSP00000257430.4:p.Ser837Ter | |
| ENST00000502371.2:c.863C>A | ||
| ENST00000507379.5:c.2456C>A | ENSP00000423224.1:p.Ser819Ter | |
| ENST00000508376.6:c.2510C>A | ENSP00000427089.2:p.Ser837Ter | |
| ENST00000508624.5:c.*1832C>A | ENSP00000424265.1:n.*1832C>A | |
| ENST00000512211.6:c.2510C>A | ENSP00000423828.2:p.Ser837Ter | |
| ENST00000520401.1:c.230+9132C>A | ||
| NM_000038.5:c.2510C>A | NP_000029.2:p.Ser837Ter | |
| NM_001127510.2:c.2510C>A | NP_001120982.1:p.Ser837Ter | |
| NM_001127511.2:c.2456C>A | NP_001120983.2:p.Ser819Ter | |
| NM_001354895.1:c.2510C>A | NP_001341824.1:p.Ser837Ter | |
| NM_001354896.1:c.2564C>A | NP_001341825.1:p.Ser855Ter | |
| NM_001354897.1:c.2540C>A | NP_001341826.1:p.Ser847Ter | |
| NM_001354898.1:c.2435C>A | NP_001341827.1:p.Ser812Ter | |
| NM_001354899.1:c.2426C>A | NP_001341828.1:p.Ser809Ter | |
| NM_001354900.1:c.2387C>A | NP_001341829.1:p.Ser796Ter | |
| NM_001354901.1:c.2333C>A | NP_001341830.1:p.Ser778Ter | |
| NM_001354902.1:c.2237C>A | NP_001341831.1:p.Ser746Ter | |
| NM_001354903.1:c.2207C>A | NP_001341832.1:p.Ser736Ter | |
| NM_001354904.1:c.2132C>A | NP_001341833.1:p.Ser711Ter | |
| NM_001354905.1:c.2030C>A | NP_001341834.1:p.Ser677Ter | |
| NM_001354906.1:c.1661C>A | NP_001341835.1:p.Ser554Ter | |
| NM_000038.6:c.2510C>A MANE Select | NP_000029.2:p.Ser837Ter | |
| NM_001127510.3:c.2510C>A | NP_001120982.1:p.Ser837Ter | |
| NM_001127511.3:c.2456C>A | NP_001120983.2:p.Ser819Ter | |
| NM_001354895.2:c.2510C>A | NP_001341824.1:p.Ser837Ter | |
| NM_001354896.2:c.2564C>A | NP_001341825.1:p.Ser855Ter | |
| NM_001354897.2:c.2540C>A | NP_001341826.1:p.Ser847Ter | |
| NM_001354898.2:c.2435C>A | NP_001341827.1:p.Ser812Ter | |
| NM_001354899.2:c.2426C>A | NP_001341828.1:p.Ser809Ter | |
| NM_001354900.2:c.2387C>A | NP_001341829.1:p.Ser796Ter | |
| NM_001354901.2:c.2333C>A | NP_001341830.1:p.Ser778Ter | |
| NM_001354902.2:c.2237C>A | NP_001341831.1:p.Ser746Ter | |
| NM_001354903.2:c.2207C>A | NP_001341832.1:p.Ser736Ter | |
| NM_001354904.2:c.2132C>A | NP_001341833.1:p.Ser711Ter | |
| NM_001354905.2:c.2030C>A | NP_001341834.1:p.Ser677Ter | |
| NM_001354906.2:c.1661C>A | NP_001341835.1:p.Ser554Ter |