Revel Score:
ENST00000324856 (MANE Select)
0.089
ENST00000457599
0.089
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.26696849G>A , CM000663.2:g.26696849G>A | GRCh38 |
| NC_000001.10:g.27023340G>A , CM000663.1:g.27023340G>A | GRCh37 |
| NC_000001.9:g.26895927G>A | NCBI36 |
| NG_029965.1:g.5819G>A , LRG_875:g.5819G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324856.13:c.446G>A MANE Select | ENSP00000320485.7:p.Gly149Asp | |
| ENST00000430799.7:c.-13+3232G>A | ENSP00000390317.3:n.-13+3232G>A | |
| ENST00000637465.1:c.-13+749G>A | ENSP00000490650.1:n.-13+749G>A | |
| ENST00000324856.11:c.446G>A | ENSP00000320485.7:p.Gly149Asp | |
| ENST00000457599.6:c.446G>A | ENSP00000387636.2:p.Gly149Asp | |
| NM_006015.4:c.446G>A , LRG_875t1:c.446G>A | NP_006006.3:p.Gly149Asp | |
| NM_139135.2:c.446G>A | NP_624361.1:p.Gly149Asp | |
| NM_006015.5:c.446G>A | NP_006006.3:p.Gly149Asp | |
| NM_139135.3:c.446G>A | NP_624361.1:p.Gly149Asp | |
| NM_006015.6:c.446G>A MANE Select | NP_006006.3:p.Gly149Asp | |
| NM_139135.4:c.446G>A | NP_624361.1:p.Gly149Asp |