Revel Score:
ENST00000311895 (MANE Select)
0.017
ENST00000389138
0.017
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.13948242C>A , CM000678.2:g.13948242C>A | GRCh38 |
| NC_000016.9:g.14042099C>A , CM000678.1:g.14042099C>A | GRCh37 |
| NC_000016.8:g.13949600C>A | NCBI36 |
| NG_011442.1:g.33086C>A , LRG_463:g.33086C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682617.1:c.2784C>A | ENSP00000507912.1:p.Asp928Glu | |
| ENST00000683962.1:c.*2340C>A | ENSP00000506854.1:n.*2340C>A | |
| ENST00000311895.8:c.2646C>A MANE Select | ENSP00000310520.7:p.Asp882Glu | |
| ENST00000311895.7:c.2646C>A | ENSP00000310520.7:p.Asp882Glu | |
| ENST00000389138.7:n.1923C>A | ||
| NM_005236.2:c.2646C>A , LRG_463t1:c.2646C>A | NP_005227.1:p.Asp882Glu | |
| XM_011522424.1:c.2784C>A | XP_011520726.1:p.Asp928Glu | |
| XM_011522425.1:c.2103C>A | XP_011520727.1:p.Asp701Glu | |
| XM_011522426.1:c.1857C>A | XP_011520728.1:p.Asp619Glu | |
| XM_011522427.1:c.1296C>A | XP_011520729.1:p.Asp432Glu | |
| XR_932805.1:n.2805C>A | ||
| XM_011522424.3:c.2784C>A | XP_011520726.1:p.Asp928Glu | |
| XM_017023043.2:c.1857C>A | XP_016878532.1:p.Asp619Glu | |
| NM_005236.3:c.2646C>A MANE Select | NP_005227.1:p.Asp882Glu |