Revel Score:
ENST00000520113 (MANE Select)
0.863
ENST00000369538
0.863
ENST00000353928
0.863
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114677923G>A , CM000663.2:g.114677923G>A | GRCh38 |
| NC_000001.10:g.115220544G>A , CM000663.1:g.115220544G>A | GRCh37 |
| NC_000001.9:g.115022067G>A | NCBI36 |
| NG_008012.1:g.22633C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369538.4:c.1199C>T | ENSP00000358551.4:p.Ala400Val | |
| ENST00000520113.7:c.1211C>T MANE Select | ENSP00000430075.3:p.Ala404Val | |
| ENST00000637080.1:c.994C>T | ENSP00000489753.1:n.994C>T | |
| ENST00000639077.1:n.876C>T | ||
| ENST00000369538.3:c.1298C>T | ENSP00000358551.3:p.Ala433Val | |
| ENST00000520113.6:c.1310C>T | ENSP00000430075.2:p.Ala437Val | |
| NM_000036.2:c.1310C>T | NP_000027.2:p.Ala437Val | |
| NM_001172626.1:c.1298C>T | NP_001166097.1:p.Ala433Val | |
| NM_000036.3:c.1211C>T MANE Select | NP_000027.3:p.Ala404Val | |
| NM_001172626.2:c.1199C>T | NP_001166097.2:p.Ala400Val |