Linked Data
ClinVar Variation Id:
216153
dbSNP Id:
rs761733547
ExAC:
5:112173381 C / T
gnomAD v2:
5-112173381-C-T
gnomAD v3:
5-112837684-C-T
gnomAD v4:
5-112837684-C-T
COSMIC:
COSM4642932
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112837684C>T , CM000667.2:g.112837684C>T | GRCh38 |
| NC_000005.9:g.112173381C>T , CM000667.1:g.112173381C>T | GRCh37 |
| NC_000005.8:g.112201280C>T | NCBI36 |
| NG_008481.4:g.150164C>T , LRG_130:g.150164C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.1755C>T | ENSP00000484935.2:n.1755C>T | |
| ENST00000504915.3:c.2144C>T | ENSP00000473355.2:p.Ala715Val | |
| ENST00000505350.2:c.*2096C>T | ENSP00000481752.1:n.*2096C>T | |
| ENST00000507379.6:c.2036C>T | ENSP00000423224.2:p.Ala679Val | |
| ENST00000509732.6:c.2090C>T | ENSP00000426541.2:p.Ala697Val | |
| ENST00000512211.7:c.2090C>T | ENSP00000423828.3:p.Ala697Val | |
| ENST00000257430.9:c.2090C>T MANE Select | ENSP00000257430.4:p.Ala697Val | |
| ENST00000257430.8:c.2090C>T | ENSP00000257430.4:p.Ala697Val | |
| ENST00000502371.2:c.443C>T | ||
| ENST00000504915.2:c.779C>T | ENSP00000473355.1:p.Ala260Val | |
| ENST00000507379.5:c.2036C>T | ENSP00000423224.1:p.Ala679Val | |
| ENST00000508376.6:c.2090C>T | ENSP00000427089.2:p.Ala697Val | |
| ENST00000508624.5:c.*1412C>T | ENSP00000424265.1:n.*1412C>T | |
| ENST00000512211.6:c.2090C>T | ENSP00000423828.2:p.Ala697Val | |
| ENST00000520401.1:c.230+8712C>T | ||
| NM_000038.5:c.2090C>T | NP_000029.2:p.Ala697Val | |
| NM_001127510.2:c.2090C>T | NP_001120982.1:p.Ala697Val | |
| NM_001127511.2:c.2036C>T | NP_001120983.2:p.Ala679Val | |
| NM_001354895.1:c.2090C>T | NP_001341824.1:p.Ala697Val | |
| NM_001354896.1:c.2144C>T | NP_001341825.1:p.Ala715Val | |
| NM_001354897.1:c.2120C>T | NP_001341826.1:p.Ala707Val | |
| NM_001354898.1:c.2015C>T | NP_001341827.1:p.Ala672Val | |
| NM_001354899.1:c.2006C>T | NP_001341828.1:p.Ala669Val | |
| NM_001354900.1:c.1967C>T | NP_001341829.1:p.Ala656Val | |
| NM_001354901.1:c.1913C>T | NP_001341830.1:p.Ala638Val | |
| NM_001354902.1:c.1817C>T | NP_001341831.1:p.Ala606Val | |
| NM_001354903.1:c.1787C>T | NP_001341832.1:p.Ala596Val | |
| NM_001354904.1:c.1712C>T | NP_001341833.1:p.Ala571Val | |
| NM_001354905.1:c.1610C>T | NP_001341834.1:p.Ala537Val | |
| NM_001354906.1:c.1241C>T | NP_001341835.1:p.Ala414Val | |
| NM_000038.6:c.2090C>T MANE Select | NP_000029.2:p.Ala697Val | |
| NM_001127510.3:c.2090C>T | NP_001120982.1:p.Ala697Val | |
| NM_001127511.3:c.2036C>T | NP_001120983.2:p.Ala679Val | |
| NM_001354895.2:c.2090C>T | NP_001341824.1:p.Ala697Val | |
| NM_001354896.2:c.2144C>T | NP_001341825.1:p.Ala715Val | |
| NM_001354897.2:c.2120C>T | NP_001341826.1:p.Ala707Val | |
| NM_001354898.2:c.2015C>T | NP_001341827.1:p.Ala672Val | |
| NM_001354899.2:c.2006C>T | NP_001341828.1:p.Ala669Val | |
| NM_001354900.2:c.1967C>T | NP_001341829.1:p.Ala656Val | |
| NM_001354901.2:c.1913C>T | NP_001341830.1:p.Ala638Val | |
| NM_001354902.2:c.1817C>T | NP_001341831.1:p.Ala606Val | |
| NM_001354903.2:c.1787C>T | NP_001341832.1:p.Ala596Val | |
| NM_001354904.2:c.1712C>T | NP_001341833.1:p.Ala571Val | |
| NM_001354905.2:c.1610C>T | NP_001341834.1:p.Ala537Val | |
| NM_001354906.2:c.1241C>T | NP_001341835.1:p.Ala414Val |