Revel Score:
ENST00000419559
0.054
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47478473A>G , CM000664.2:g.47478473A>G | GRCh38 |
| NC_000002.11:g.47705612A>G , CM000664.1:g.47705612A>G | GRCh37 |
| NC_000002.10:g.47559116A>G | NCBI36 |
| NG_007110.2:g.80350A>G , LRG_218:g.80350A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644900.2:c.2412A>G | ENSP00000495641.2:p.Ala804= | |
| ENST00000233146.7:c.2412A>G MANE Select | ENSP00000233146.2:p.Ala804= | |
| ENST00000543555.6:c.2214A>G | ENSP00000442697.1:p.Ala738= | |
| ENST00000644092.1:c.*712A>G | ENSP00000496351.1:n.*712A>G | |
| ENST00000644900.1:c.265A>G | ||
| ENST00000645339.1:c.2412A>G | ENSP00000496441.1:p.Ala804= | |
| ENST00000645506.1:c.2412A>G | ENSP00000495455.1:p.Ala804= | |
| ENST00000646415.1:c.2412A>G | ENSP00000495543.1:p.Ala804= | |
| ENST00000233146.6:c.2412A>G | ENSP00000233146.2:p.Ala804= | |
| ENST00000406134.5:c.2412A>G | ENSP00000384199.1:p.Ala804= | |
| ENST00000543555.5:c.2214A>G | ENSP00000442697.1:p.Ala738= | |
| ENST00000610696.4:c.*808A>G | ENSP00000483159.1:n.*808A>G | |
| ENST00000613514.4:c.*952A>G | ENSP00000484137.1:n.*952A>G | |
| ENST00000617333.3:c.*1178A>G | ENSP00000482468.1:n.*1178A>G | |
| ENST00000617938.4:c.*1384A>G | ENSP00000481158.1:n.*1384A>G | |
| ENST00000621359.2:c.2411A>G | ENSP00000481416.1:p.His804Arg | |
| NM_000251.2:c.2412A>G , LRG_218t1:c.2412A>G | NP_000242.1:p.Ala804= | |
| NM_001258281.1:c.2214A>G | NP_001245210.1:p.Ala738= | |
| XM_005264332.2:c.2412A>G | XP_005264389.2:p.Ala804= | |
| XM_011532867.1:c.2412A>G | XP_011531169.1:p.Ala804= | |
| XR_939685.1:n.2484A>G | ||
| XM_005264332.4:c.2412A>G | XP_005264389.2:p.Ala804= | |
| XM_011532867.2:c.2412A>G | XP_011531169.1:p.Ala804= | |
| XR_001738747.2:n.2474A>G | ||
| XR_939685.2:n.2474A>G | ||
| NM_000251.3:c.2412A>G MANE Select | NP_000242.1:p.Ala804= |