Revel Score:
ENST00000288602
0.508
ENST00000496384
0.420
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140734715G>A , CM000669.2:g.140734715G>A | GRCh38 |
| NC_000007.13:g.140434515G>A , CM000669.1:g.140434515G>A | GRCh37 |
| NC_000007.12:g.140080984G>A | NCBI36 |
| NG_007873.3:g.195050C>T , LRG_299:g.195050C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.2183C>T MANE Select | ENSP00000493543.1:p.Ala728Val | |
| ENST00000288602.11:c.2303C>T | ENSP00000288602.7:p.Ala768Val | |
| ENST00000479537.6:c.935C>T | ||
| ENST00000496384.7:c.2183C>T | ENSP00000419060.2:p.Ala728Val | |
| ENST00000497784.2:c.*1633C>T | ENSP00000420119.2:n.*1633C>T | |
| ENST00000642228.1:c.*1261C>T | ENSP00000493678.1:n.*1261C>T | |
| ENST00000642875.1:n.1581C>T | ||
| ENST00000644120.1:n.2517+5097C>T | ||
| ENST00000644650.1:c.1482C>T | ||
| ENST00000644905.1:n.3065C>T | ||
| ENST00000644969.2:c.2303C>T MANE Plus Clinical | ENSP00000496776.1:p.Ala768Val | |
| ENST00000645443.1:n.1962C>T | ||
| ENST00000646730.1:c.*841C>T | ENSP00000494784.1:n.*841C>T | |
| ENST00000646891.1:c.2183C>T | ENSP00000493543.1:p.Ala728Val | |
| ENST00000647434.1:c.1060C>T | ENSP00000495132.1:n.1060C>T | |
| ENST00000288602.10:c.2183C>T | ENSP00000288602.6:p.Ala728Val | |
| ENST00000479537.5:c.549C>T | ENSP00000418033.1:n.549C>T | |
| ENST00000496384.6:c.1006C>T | ||
| ENST00000497784.1:c.2218C>T | ENSP00000420119.1:n.2218C>T | |
| NM_004333.4:c.2183C>T , LRG_299t1:c.2183C>T | NP_004324.2:p.Ala728Val | |
| XM_005250045.1:c.2183C>T | XP_005250102.1:p.Ala728Val | |
| XM_005250046.1:c.2127+5097C>T | XP_005250103.1:n.2127+5097C>T | |
| XM_011516529.1:c.2127+5097C>T | XP_011514831.1:n.2127+5097C>T | |
| XR_242190.1:n.2273C>T | ||
| XR_927520.1:n.2312C>T | ||
| XR_927521.1:n.2394C>T | ||
| XR_927522.1:n.2025C>T | ||
| XR_927523.1:n.2107C>T | ||
| NM_001354609.1:c.2183C>T | NP_001341538.1:p.Ala728Val | |
| NM_004333.5:c.2183C>T | NP_004324.2:p.Ala728Val | |
| NR_148928.1:n.3281C>T | ||
| XM_017012558.1:c.2303C>T | XP_016868047.1:p.Ala768Val | |
| XM_017012559.1:c.2247+5097C>T | XP_016868048.1:n.2247+5097C>T | |
| XR_001744857.1:n.2393C>T | ||
| XR_001744858.1:n.2145C>T | ||
| NM_001354609.2:c.2183C>T | NP_001341538.1:p.Ala728Val | |
| NM_001374244.1:c.2303C>T | NP_001361173.1:p.Ala768Val | |
| NM_001374258.1:c.2303C>T MANE Plus Clinical | NP_001361187.1:p.Ala768Val | |
| NM_004333.6:c.2183C>T MANE Select | NP_004324.2:p.Ala728Val | |
| NM_001378467.1:c.2192C>T | NP_001365396.1:p.Ala731Val | |
| NM_001378468.1:c.2127+5097C>T | NP_001365397.1:n.2127+5097C>T | |
| NM_001378469.1:c.2117C>T | NP_001365398.1:p.Ala706Val | |
| NM_001378470.1:c.2081C>T | NP_001365399.1:p.Ala694Val | |
| NM_001378471.1:c.2072C>T | NP_001365400.1:p.Ala691Val | |
| NM_001378472.1:c.2027C>T | NP_001365401.1:p.Ala676Val | |
| NM_001378473.1:c.2027C>T | NP_001365402.1:p.Ala676Val | |
| NM_001378474.1:c.2127+5097C>T | NP_001365403.1:n.2127+5097C>T | |
| NM_001378475.1:c.1919C>T | NP_001365404.1:p.Ala640Val |