Linked Data
ClinVar Variation Id:
438883
dbSNP Id:
rs764527706
COSMIC:
COSM13122
PubMed:
PMID:14966376
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112842090C>T , CM000667.2:g.112842090C>T | GRCh38 |
| NC_000005.9:g.112177787C>T , CM000667.1:g.112177787C>T | GRCh37 |
| NC_000005.8:g.112205686C>T | NCBI36 |
| NG_008481.4:g.154570C>T , LRG_130:g.154570C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.6550C>T | ENSP00000473355.2:p.Arg2184Ter | |
| ENST00000505350.2:c.*6502C>T | ENSP00000481752.1:n.*6502C>T | |
| ENST00000507379.6:c.6442C>T | ENSP00000423224.2:p.Arg2148Ter | |
| ENST00000509732.6:c.6496C>T | ENSP00000426541.2:p.Arg2166Ter | |
| ENST00000512211.7:c.6496C>T | ENSP00000423828.3:p.Arg2166Ter | |
| ENST00000257430.9:c.6496C>T MANE Select | ENSP00000257430.4:p.Arg2166Ter | |
| ENST00000257430.8:c.6496C>T | ENSP00000257430.4:p.Arg2166Ter | |
| ENST00000508376.6:c.6496C>T | ENSP00000427089.2:p.Arg2166Ter | |
| ENST00000508624.5:c.*5818C>T | ENSP00000424265.1:n.*5818C>T | |
| ENST00000520401.1:c.230+13118C>T | ||
| NM_000038.5:c.6496C>T | NP_000029.2:p.Arg2166Ter | |
| NM_001127510.2:c.6496C>T | NP_001120982.1:p.Arg2166Ter | |
| NM_001127511.2:c.6442C>T | NP_001120983.2:p.Arg2148Ter | |
| NM_001354895.1:c.6496C>T | NP_001341824.1:p.Arg2166Ter | |
| NM_001354896.1:c.6550C>T | NP_001341825.1:p.Arg2184Ter | |
| NM_001354897.1:c.6526C>T | NP_001341826.1:p.Arg2176Ter | |
| NM_001354898.1:c.6421C>T | NP_001341827.1:p.Arg2141Ter | |
| NM_001354899.1:c.6412C>T | NP_001341828.1:p.Arg2138Ter | |
| NM_001354900.1:c.6373C>T | NP_001341829.1:p.Arg2125Ter | |
| NM_001354901.1:c.6319C>T | NP_001341830.1:p.Arg2107Ter | |
| NM_001354902.1:c.6223C>T | NP_001341831.1:p.Arg2075Ter | |
| NM_001354903.1:c.6193C>T | NP_001341832.1:p.Arg2065Ter | |
| NM_001354904.1:c.6118C>T | NP_001341833.1:p.Arg2040Ter | |
| NM_001354905.1:c.6016C>T | NP_001341834.1:p.Arg2006Ter | |
| NM_001354906.1:c.5647C>T | NP_001341835.1:p.Arg1883Ter | |
| NM_000038.6:c.6496C>T MANE Select | NP_000029.2:p.Arg2166Ter | |
| NM_001127510.3:c.6496C>T | NP_001120982.1:p.Arg2166Ter | |
| NM_001127511.3:c.6442C>T | NP_001120983.2:p.Arg2148Ter | |
| NM_001354895.2:c.6496C>T | NP_001341824.1:p.Arg2166Ter | |
| NM_001354896.2:c.6550C>T | NP_001341825.1:p.Arg2184Ter | |
| NM_001354897.2:c.6526C>T | NP_001341826.1:p.Arg2176Ter | |
| NM_001354898.2:c.6421C>T | NP_001341827.1:p.Arg2141Ter | |
| NM_001354899.2:c.6412C>T | NP_001341828.1:p.Arg2138Ter | |
| NM_001354900.2:c.6373C>T | NP_001341829.1:p.Arg2125Ter | |
| NM_001354901.2:c.6319C>T | NP_001341830.1:p.Arg2107Ter | |
| NM_001354902.2:c.6223C>T | NP_001341831.1:p.Arg2075Ter | |
| NM_001354903.2:c.6193C>T | NP_001341832.1:p.Arg2065Ter | |
| NM_001354904.2:c.6118C>T | NP_001341833.1:p.Arg2040Ter | |
| NM_001354905.2:c.6016C>T | NP_001341834.1:p.Arg2006Ter | |
| NM_001354906.2:c.5647C>T | NP_001341835.1:p.Arg1883Ter |