Revel Score:
ENST00000284061 (MANE Select)
0.774
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.56848773G>T , CM000679.2:g.56848773G>T | GRCh38 |
| NC_000017.10:g.54926134G>T , CM000679.1:g.54926134G>T | GRCh37 |
| NC_000017.9:g.52281133G>T | NCBI36 |
| NG_033888.1:g.19675G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284061.8:c.966G>T (DGKE) MANE Select | ENSP00000284061.3:p.Trp322Cys | |
| ENST00000648772.1:c.*313+3170C>A (TRIM25) | ENSP00000498158.1:n.*313+3170C>A | |
| ENST00000284061.7:c.966G>T (DGKE) | ENSP00000284061.3:p.Trp322Cys | |
| ENST00000572944.1:c.796G>T (DGKE) | ||
| NM_003647.2:c.966G>T (DGKE) | NP_003638.1:p.Trp322Cys | |
| XM_011525394.1:c.1020G>T (DGKE) | XP_011523696.1:p.Trp340Cys | |
| XM_011525395.1:c.1020G>T (DGKE) | XP_011523697.1:p.Trp340Cys | |
| XM_011525396.1:c.1020G>T (DGKE) | XP_011523698.1:p.Trp340Cys | |
| XM_011525397.1:c.1020G>T (DGKE) | XP_011523699.1:p.Trp340Cys | |
| XM_011525398.1:c.510G>T (DGKE) | XP_011523700.1:p.Trp170Cys | |
| XR_934581.1:n.1119G>T (DGKE) | ||
| XM_011525394.3:c.1020G>T (DGKE) | XP_011523696.1:p.Trp340Cys | |
| XM_011525395.2:c.1020G>T (DGKE) | XP_011523697.1:p.Trp340Cys | |
| XM_011525396.2:c.1020G>T (DGKE) | XP_011523698.1:p.Trp340Cys | |
| XM_017025243.2:c.1338G>T (DGKE) | XP_016880732.1:p.Trp446Cys | |
| XM_017025244.2:c.1020G>T (DGKE) | XP_016880733.1:p.Trp340Cys | |
| XR_001752670.2:n.1524G>T (DGKE) | ||
| XR_001752671.1:n.1131G>T (DGKE) | ||
| XR_001752672.1:n.1132G>T (DGKE) | ||
| XR_002958079.1:n.1130G>T (DGKE) | ||
| NM_003647.3:c.966G>T (DGKE) MANE Select | NP_003638.1:p.Trp322Cys |