Linked Data
ClinVar Variation Id:
140954
dbSNP Id:
rs587778044
ExAC:
5:112179437 G / A
gnomAD v2:
5-112179437-G-A
gnomAD v3:
5-112843740-G-A
gnomAD v4:
5-112843740-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112843740G>A , CM000667.2:g.112843740G>A | GRCh38 |
| NC_000005.9:g.112179437G>A , CM000667.1:g.112179437G>A | GRCh37 |
| NC_000005.8:g.112207336G>A | NCBI36 |
| NG_008481.4:g.156220G>A , LRG_130:g.156220G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.8200G>A | ENSP00000473355.2:p.Val2734Met | |
| ENST00000505350.2:c.*8152G>A | ENSP00000481752.1:n.*8152G>A | |
| ENST00000507379.6:c.8092G>A | ENSP00000423224.2:p.Val2698Met | |
| ENST00000509732.6:c.8146G>A | ENSP00000426541.2:p.Val2716Met | |
| ENST00000512211.7:c.8146G>A | ENSP00000423828.3:p.Val2716Met | |
| ENST00000257430.9:c.8146G>A MANE Select | ENSP00000257430.4:p.Val2716Met | |
| ENST00000257430.8:c.8146G>A | ENSP00000257430.4:p.Val2716Met | |
| ENST00000508376.6:c.8146G>A | ENSP00000427089.2:p.Val2716Met | |
| ENST00000520401.1:c.231-12909G>A | ||
| NM_000038.5:c.8146G>A | NP_000029.2:p.Val2716Met | |
| NM_001127510.2:c.8146G>A | NP_001120982.1:p.Val2716Met | |
| NM_001127511.2:c.8092G>A | NP_001120983.2:p.Val2698Met | |
| NM_001354895.1:c.8146G>A | NP_001341824.1:p.Val2716Met | |
| NM_001354896.1:c.8200G>A | NP_001341825.1:p.Val2734Met | |
| NM_001354897.1:c.8176G>A | NP_001341826.1:p.Val2726Met | |
| NM_001354898.1:c.8071G>A | NP_001341827.1:p.Val2691Met | |
| NM_001354899.1:c.8062G>A | NP_001341828.1:p.Val2688Met | |
| NM_001354900.1:c.8023G>A | NP_001341829.1:p.Val2675Met | |
| NM_001354901.1:c.7969G>A | NP_001341830.1:p.Val2657Met | |
| NM_001354902.1:c.7873G>A | NP_001341831.1:p.Val2625Met | |
| NM_001354903.1:c.7843G>A | NP_001341832.1:p.Val2615Met | |
| NM_001354904.1:c.7768G>A | NP_001341833.1:p.Val2590Met | |
| NM_001354905.1:c.7666G>A | NP_001341834.1:p.Val2556Met | |
| NM_001354906.1:c.7297G>A | NP_001341835.1:p.Val2433Met | |
| NM_000038.6:c.8146G>A MANE Select | NP_000029.2:p.Val2716Met | |
| NM_001127510.3:c.8146G>A | NP_001120982.1:p.Val2716Met | |
| NM_001127511.3:c.8092G>A | NP_001120983.2:p.Val2698Met | |
| NM_001354895.2:c.8146G>A | NP_001341824.1:p.Val2716Met | |
| NM_001354896.2:c.8200G>A | NP_001341825.1:p.Val2734Met | |
| NM_001354897.2:c.8176G>A | NP_001341826.1:p.Val2726Met | |
| NM_001354898.2:c.8071G>A | NP_001341827.1:p.Val2691Met | |
| NM_001354899.2:c.8062G>A | NP_001341828.1:p.Val2688Met | |
| NM_001354900.2:c.8023G>A | NP_001341829.1:p.Val2675Met | |
| NM_001354901.2:c.7969G>A | NP_001341830.1:p.Val2657Met | |
| NM_001354902.2:c.7873G>A | NP_001341831.1:p.Val2625Met | |
| NM_001354903.2:c.7843G>A | NP_001341832.1:p.Val2615Met | |
| NM_001354904.2:c.7768G>A | NP_001341833.1:p.Val2590Met | |
| NM_001354905.2:c.7666G>A | NP_001341834.1:p.Val2556Met | |
| NM_001354906.2:c.7297G>A | NP_001341835.1:p.Val2433Met |