Linked Data
ClinVar Variation Id:
1510117
ClinVar RCV Id:
RCV003745523
dbSNP Id:
rs1195229686
gnomAD v2:
5-112154919-A-C
gnomAD v4:
5-112819222-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112819222A>C , CM000667.2:g.112819222A>C | GRCh38 |
| NC_000005.9:g.112154919A>C , CM000667.1:g.112154919A>C | GRCh37 |
| NC_000005.8:g.112182818A>C | NCBI36 |
| NG_008481.4:g.131702A>C , LRG_130:g.131702A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.1190A>C | ENSP00000484935.2:p.Asp397Ala | |
| ENST00000504915.3:c.1190A>C | ENSP00000473355.2:p.Asp397Ala | |
| ENST00000505084.2:n.1246A>C | ||
| ENST00000505350.2:c.*1196A>C | ENSP00000481752.1:n.*1196A>C | |
| ENST00000507379.6:c.1136A>C | ENSP00000423224.2:p.Asp379Ala | |
| ENST00000509732.6:c.1190A>C | ENSP00000426541.2:p.Asp397Ala | |
| ENST00000512211.7:c.1190A>C | ENSP00000423828.3:p.Asp397Ala | |
| ENST00000257430.9:c.1190A>C MANE Select | ENSP00000257430.4:p.Asp397Ala | |
| ENST00000257430.8:c.1190A>C | ENSP00000257430.4:p.Asp397Ala | |
| ENST00000507379.5:c.1136A>C | ENSP00000423224.1:p.Asp379Ala | |
| ENST00000508376.6:c.1190A>C | ENSP00000427089.2:p.Asp397Ala | |
| ENST00000508624.5:c.*512A>C | ENSP00000424265.1:n.*512A>C | |
| ENST00000512211.6:c.1190A>C | ENSP00000423828.2:p.Asp397Ala | |
| NM_000038.5:c.1190A>C | NP_000029.2:p.Asp397Ala | |
| NM_001127510.2:c.1190A>C | NP_001120982.1:p.Asp397Ala | |
| NM_001127511.2:c.1136A>C | NP_001120983.2:p.Asp379Ala | |
| NM_001354895.1:c.1190A>C | NP_001341824.1:p.Asp397Ala | |
| NM_001354896.1:c.1190A>C | NP_001341825.1:p.Asp397Ala | |
| NM_001354897.1:c.1220A>C | NP_001341826.1:p.Asp407Ala | |
| NM_001354898.1:c.1115A>C | NP_001341827.1:p.Asp372Ala | |
| NM_001354899.1:c.1106A>C | NP_001341828.1:p.Asp369Ala | |
| NM_001354900.1:c.1013A>C | NP_001341829.1:p.Asp338Ala | |
| NM_001354901.1:c.1013A>C | NP_001341830.1:p.Asp338Ala | |
| NM_001354902.1:c.964-47A>C | NP_001341831.1:n.964-47A>C | |
| NM_001354903.1:c.934-47A>C | NP_001341832.1:n.934-47A>C | |
| NM_001354904.1:c.859-47A>C | NP_001341833.1:n.859-47A>C | |
| NM_001354905.1:c.757-47A>C | NP_001341834.1:n.757-47A>C | |
| NM_001354906.1:c.341A>C | NP_001341835.1:p.Asp114Ala | |
| NM_000038.6:c.1190A>C MANE Select | NP_000029.2:p.Asp397Ala | |
| NM_001127510.3:c.1190A>C | NP_001120982.1:p.Asp397Ala | |
| NM_001127511.3:c.1136A>C | NP_001120983.2:p.Asp379Ala | |
| NM_001354895.2:c.1190A>C | NP_001341824.1:p.Asp397Ala | |
| NM_001354896.2:c.1190A>C | NP_001341825.1:p.Asp397Ala | |
| NM_001354897.2:c.1220A>C | NP_001341826.1:p.Asp407Ala | |
| NM_001354898.2:c.1115A>C | NP_001341827.1:p.Asp372Ala | |
| NM_001354899.2:c.1106A>C | NP_001341828.1:p.Asp369Ala | |
| NM_001354900.2:c.1013A>C | NP_001341829.1:p.Asp338Ala | |
| NM_001354901.2:c.1013A>C | NP_001341830.1:p.Asp338Ala | |
| NM_001354902.2:c.964-47A>C | NP_001341831.1:n.964-47A>C | |
| NM_001354903.2:c.934-47A>C | NP_001341832.1:n.934-47A>C | |
| NM_001354904.2:c.859-47A>C | NP_001341833.1:n.859-47A>C | |
| NM_001354905.2:c.757-47A>C | NP_001341834.1:n.757-47A>C | |
| NM_001354906.2:c.341A>C | NP_001341835.1:p.Asp114Ala |