Linked Data
ClinVar Variation Id:
184937
dbSNP Id:
rs775126020
gnomAD v4:
5-112819026-C-T
COSMIC:
COSM19239
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112819026C>T , CM000667.2:g.112819026C>T | GRCh38 |
| NC_000005.9:g.112154723C>T , CM000667.1:g.112154723C>T | GRCh37 |
| NC_000005.8:g.112182622C>T | NCBI36 |
| NG_008481.4:g.131506C>T , LRG_130:g.131506C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.994C>T | ENSP00000484935.2:p.Arg332Ter | |
| ENST00000504915.3:c.994C>T | ENSP00000473355.2:p.Arg332Ter | |
| ENST00000505084.2:n.1050C>T | ||
| ENST00000505350.2:c.*1000C>T | ENSP00000481752.1:n.*1000C>T | |
| ENST00000507379.6:c.940C>T | ENSP00000423224.2:p.Arg314Ter | |
| ENST00000509732.6:c.994C>T | ENSP00000426541.2:p.Arg332Ter | |
| ENST00000512211.7:c.994C>T | ENSP00000423828.3:p.Arg332Ter | |
| ENST00000257430.9:c.994C>T MANE Select | ENSP00000257430.4:p.Arg332Ter | |
| ENST00000257430.8:c.994C>T | ENSP00000257430.4:p.Arg332Ter | |
| ENST00000507379.5:c.940C>T | ENSP00000423224.1:p.Arg314Ter | |
| ENST00000508376.6:c.994C>T | ENSP00000427089.2:p.Arg332Ter | |
| ENST00000508624.5:c.*316C>T | ENSP00000424265.1:n.*316C>T | |
| ENST00000512211.6:c.994C>T | ENSP00000423828.2:p.Arg332Ter | |
| NM_000038.5:c.994C>T | NP_000029.2:p.Arg332Ter | |
| NM_001127510.2:c.994C>T | NP_001120982.1:p.Arg332Ter | |
| NM_001127511.2:c.940C>T | NP_001120983.2:p.Arg314Ter | |
| NM_001354895.1:c.994C>T | NP_001341824.1:p.Arg332Ter | |
| NM_001354896.1:c.994C>T | NP_001341825.1:p.Arg332Ter | |
| NM_001354897.1:c.1024C>T | NP_001341826.1:p.Arg342Ter | |
| NM_001354898.1:c.919C>T | NP_001341827.1:p.Arg307Ter | |
| NM_001354899.1:c.910C>T | NP_001341828.1:p.Arg304Ter | |
| NM_001354900.1:c.817C>T | NP_001341829.1:p.Arg273Ter | |
| NM_001354901.1:c.817C>T | NP_001341830.1:p.Arg273Ter | |
| NM_001354902.1:c.964-243C>T | NP_001341831.1:n.964-243C>T | |
| NM_001354903.1:c.934-243C>T | NP_001341832.1:n.934-243C>T | |
| NM_001354904.1:c.859-243C>T | NP_001341833.1:n.859-243C>T | |
| NM_001354905.1:c.757-243C>T | NP_001341834.1:n.757-243C>T | |
| NM_001354906.1:c.145C>T | NP_001341835.1:p.Arg49Ter | |
| NM_000038.6:c.994C>T MANE Select | NP_000029.2:p.Arg332Ter | |
| NM_001127510.3:c.994C>T | NP_001120982.1:p.Arg332Ter | |
| NM_001127511.3:c.940C>T | NP_001120983.2:p.Arg314Ter | |
| NM_001354895.2:c.994C>T | NP_001341824.1:p.Arg332Ter | |
| NM_001354896.2:c.994C>T | NP_001341825.1:p.Arg332Ter | |
| NM_001354897.2:c.1024C>T | NP_001341826.1:p.Arg342Ter | |
| NM_001354898.2:c.919C>T | NP_001341827.1:p.Arg307Ter | |
| NM_001354899.2:c.910C>T | NP_001341828.1:p.Arg304Ter | |
| NM_001354900.2:c.817C>T | NP_001341829.1:p.Arg273Ter | |
| NM_001354901.2:c.817C>T | NP_001341830.1:p.Arg273Ter | |
| NM_001354902.2:c.964-243C>T | NP_001341831.1:n.964-243C>T | |
| NM_001354903.2:c.934-243C>T | NP_001341832.1:n.934-243C>T | |
| NM_001354904.2:c.859-243C>T | NP_001341833.1:n.859-243C>T | |
| NM_001354905.2:c.757-243C>T | NP_001341834.1:n.757-243C>T | |
| NM_001354906.2:c.145C>T | NP_001341835.1:p.Arg49Ter |