Linked Data
ClinVar Variation Id:
162794
dbSNP Id:
rs727502903
gnomAD v2:
7-140434390-A-G
gnomAD v3:
7-140734590-A-G
gnomAD v4:
7-140734590-A-G
ERepo:
CA175333/MONDO:0021060/004
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140734590A>G , CM000669.2:g.140734590A>G | GRCh38 |
| NC_000007.13:g.140434390A>G , CM000669.1:g.140434390A>G | GRCh37 |
| NC_000007.12:g.140080859A>G | NCBI36 |
| NG_007873.3:g.195175T>C , LRG_299:g.195175T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.*7T>C MANE Select | ENSP00000493543.1:n.*7T>C | |
| ENST00000288602.11:c.*7T>C | ENSP00000288602.7:n.*7T>C | |
| ENST00000479537.6:c.1060T>C | ||
| ENST00000496384.7:c.2281+27T>C | ENSP00000419060.2:n.2281+27T>C | |
| ENST00000642228.1:c.*1386T>C | ENSP00000493678.1:n.*1386T>C | |
| ENST00000642875.1:n.1679+27T>C | ||
| ENST00000644120.1:n.2517+5222T>C | ||
| ENST00000644650.1:c.1607T>C | ||
| ENST00000644905.1:n.3190T>C | ||
| ENST00000644969.2:c.2401+27T>C MANE Plus Clinical | ENSP00000496776.1:n.2401+27T>C | |
| ENST00000645443.1:n.2087T>C | ||
| ENST00000646730.1:c.*966T>C | ENSP00000494784.1:n.*966T>C | |
| ENST00000646891.1:c.*7T>C | ENSP00000493543.1:n.*7T>C | |
| ENST00000647434.1:c.1185T>C | ENSP00000495132.1:n.1185T>C | |
| ENST00000288602.10:c.*7T>C | ENSP00000288602.6:n.*7T>C | |
| ENST00000479537.5:c.674T>C | ENSP00000418033.1:n.674T>C | |
| ENST00000496384.6:c.1104+27T>C | ||
| NM_004333.4:c.*7T>C , LRG_299t1:c.*7T>C | NP_004324.2:n.*7T>C | |
| XM_005250045.1:c.2281+27T>C | XP_005250102.1:n.2281+27T>C | |
| XM_005250046.1:c.2127+5222T>C | XP_005250103.1:n.2127+5222T>C | |
| XM_011516529.1:c.2127+5222T>C | XP_011514831.1:n.2127+5222T>C | |
| XR_242190.1:n.2398T>C | ||
| XR_927520.1:n.2437T>C | ||
| XR_927521.1:n.2519T>C | ||
| XR_927522.1:n.2150T>C | ||
| XR_927523.1:n.2232T>C | ||
| NM_001354609.1:c.2281+27T>C | NP_001341538.1:n.2281+27T>C | |
| NM_004333.5:c.*7T>C | NP_004324.2:n.*7T>C | |
| NR_148928.1:n.3406T>C | ||
| XM_017012558.1:c.2401+27T>C | XP_016868047.1:n.2401+27T>C | |
| XM_017012559.1:c.2247+5222T>C | XP_016868048.1:n.2247+5222T>C | |
| XR_001744857.1:n.2518T>C | ||
| XR_001744858.1:n.2243+27T>C | ||
| NM_001354609.2:c.2281+27T>C | NP_001341538.1:n.2281+27T>C | |
| NM_001374244.1:c.*7T>C | NP_001361173.1:n.*7T>C | |
| NM_001374258.1:c.2401+27T>C MANE Plus Clinical | NP_001361187.1:n.2401+27T>C | |
| NM_004333.6:c.*7T>C MANE Select | NP_004324.2:n.*7T>C | |
| NM_001378467.1:c.2290+27T>C | NP_001365396.1:n.2290+27T>C | |
| NM_001378468.1:c.2127+5222T>C | NP_001365397.1:n.2127+5222T>C | |
| NM_001378469.1:c.*7T>C | NP_001365398.1:n.*7T>C | |
| NM_001378470.1:c.2179+27T>C | NP_001365399.1:n.2179+27T>C | |
| NM_001378471.1:c.2170+27T>C | NP_001365400.1:n.2170+27T>C | |
| NM_001378472.1:c.2125+27T>C | NP_001365401.1:n.2125+27T>C | |
| NM_001378473.1:c.*7T>C | NP_001365402.1:n.*7T>C | |
| NM_001378474.1:c.2127+5222T>C | NP_001365403.1:n.2127+5222T>C | |
| NM_001378475.1:c.2017+27T>C | NP_001365404.1:n.2017+27T>C |