Linked Data
ClinVar Variation Id:
433653
dbSNP Id:
rs77056664
COSMIC:
COSM4166468
PubMed:
PMID:10083733
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112839360C>T , CM000667.2:g.112839360C>T | GRCh38 |
| NC_000005.9:g.112175057C>T , CM000667.1:g.112175057C>T | GRCh37 |
| NC_000005.8:g.112202956C>T | NCBI36 |
| NG_008481.4:g.151840C>T , LRG_130:g.151840C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.3431C>T | ENSP00000484935.2:n.3431C>T | |
| ENST00000504915.3:c.3820C>T | ENSP00000473355.2:p.Gln1274Ter | |
| ENST00000505350.2:c.*3772C>T | ENSP00000481752.1:n.*3772C>T | |
| ENST00000507379.6:c.3712C>T | ENSP00000423224.2:p.Gln1238Ter | |
| ENST00000509732.6:c.3766C>T | ENSP00000426541.2:p.Gln1256Ter | |
| ENST00000512211.7:c.3766C>T | ENSP00000423828.3:p.Gln1256Ter | |
| ENST00000257430.9:c.3766C>T MANE Select | ENSP00000257430.4:p.Gln1256Ter | |
| ENST00000257430.8:c.3766C>T | ENSP00000257430.4:p.Gln1256Ter | |
| ENST00000502371.2:c.2119C>T | ||
| ENST00000508376.6:c.3766C>T | ENSP00000427089.2:p.Gln1256Ter | |
| ENST00000508624.5:c.*3088C>T | ENSP00000424265.1:n.*3088C>T | |
| ENST00000512211.6:c.3766C>T | ENSP00000423828.2:p.Gln1256Ter | |
| ENST00000520401.1:c.230+10388C>T | ||
| NM_000038.5:c.3766C>T | NP_000029.2:p.Gln1256Ter | |
| NM_001127510.2:c.3766C>T | NP_001120982.1:p.Gln1256Ter | |
| NM_001127511.2:c.3712C>T | NP_001120983.2:p.Gln1238Ter | |
| NM_001354895.1:c.3766C>T | NP_001341824.1:p.Gln1256Ter | |
| NM_001354896.1:c.3820C>T | NP_001341825.1:p.Gln1274Ter | |
| NM_001354897.1:c.3796C>T | NP_001341826.1:p.Gln1266Ter | |
| NM_001354898.1:c.3691C>T | NP_001341827.1:p.Gln1231Ter | |
| NM_001354899.1:c.3682C>T | NP_001341828.1:p.Gln1228Ter | |
| NM_001354900.1:c.3643C>T | NP_001341829.1:p.Gln1215Ter | |
| NM_001354901.1:c.3589C>T | NP_001341830.1:p.Gln1197Ter | |
| NM_001354902.1:c.3493C>T | NP_001341831.1:p.Gln1165Ter | |
| NM_001354903.1:c.3463C>T | NP_001341832.1:p.Gln1155Ter | |
| NM_001354904.1:c.3388C>T | NP_001341833.1:p.Gln1130Ter | |
| NM_001354905.1:c.3286C>T | NP_001341834.1:p.Gln1096Ter | |
| NM_001354906.1:c.2917C>T | NP_001341835.1:p.Gln973Ter | |
| NM_000038.6:c.3766C>T MANE Select | NP_000029.2:p.Gln1256Ter | |
| NM_001127510.3:c.3766C>T | NP_001120982.1:p.Gln1256Ter | |
| NM_001127511.3:c.3712C>T | NP_001120983.2:p.Gln1238Ter | |
| NM_001354895.2:c.3766C>T | NP_001341824.1:p.Gln1256Ter | |
| NM_001354896.2:c.3820C>T | NP_001341825.1:p.Gln1274Ter | |
| NM_001354897.2:c.3796C>T | NP_001341826.1:p.Gln1266Ter | |
| NM_001354898.2:c.3691C>T | NP_001341827.1:p.Gln1231Ter | |
| NM_001354899.2:c.3682C>T | NP_001341828.1:p.Gln1228Ter | |
| NM_001354900.2:c.3643C>T | NP_001341829.1:p.Gln1215Ter | |
| NM_001354901.2:c.3589C>T | NP_001341830.1:p.Gln1197Ter | |
| NM_001354902.2:c.3493C>T | NP_001341831.1:p.Gln1165Ter | |
| NM_001354903.2:c.3463C>T | NP_001341832.1:p.Gln1155Ter | |
| NM_001354904.2:c.3388C>T | NP_001341833.1:p.Gln1130Ter | |
| NM_001354905.2:c.3286C>T | NP_001341834.1:p.Gln1096Ter | |
| NM_001354906.2:c.2917C>T | NP_001341835.1:p.Gln973Ter |