Canonical Allele Identifier: CA399905617

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56856560G>A , CM000679.2:g.56856560G>A GRCh38
NC_000017.10:g.54933921G>A , CM000679.1:g.54933921G>A GRCh37
NC_000017.9:g.52288920G>A NCBI36
NG_033888.1:g.27462G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682766.1:c.1364-1450C>T (TRIM25) ENSP00000507876.1:n.1364-1450C>T
ENST00000284061.8:c.1147G>A (DGKE) MANE Select ENSP00000284061.3:p.Ala383Thr
ENST00000648772.1:c.1364-1450C>T (TRIM25) ENSP00000498158.1:n.1364-1450C>T
ENST00000284061.7:c.1147G>A (DGKE) ENSP00000284061.3:p.Ala383Thr
ENST00000572944.1:c.977G>A (DGKE)
NM_003647.2:c.1147G>A (DGKE) NP_003638.1:p.Ala383Thr
XM_011525394.1:c.1201G>A (DGKE) XP_011523696.1:p.Ala401Thr
XM_011525395.1:c.1201G>A (DGKE) XP_011523697.1:p.Ala401Thr
XM_011525396.1:c.1201G>A (DGKE) XP_011523698.1:p.Ala401Thr
XM_011525397.1:c.1201G>A (DGKE) XP_011523699.1:p.Ala401Thr
XM_011525398.1:c.691G>A (DGKE) XP_011523700.1:p.Ala231Thr
XR_934581.1:n.1300G>A (DGKE)
XM_011525394.3:c.1201G>A (DGKE) XP_011523696.1:p.Ala401Thr
XM_011525395.2:c.1201G>A (DGKE) XP_011523697.1:p.Ala401Thr
XM_011525396.2:c.1201G>A (DGKE) XP_011523698.1:p.Ala401Thr
XM_017025243.2:c.1519G>A (DGKE) XP_016880732.1:p.Ala507Thr
XM_017025244.2:c.1201G>A (DGKE) XP_016880733.1:p.Ala401Thr
XR_001752670.2:n.1705G>A (DGKE)
XR_001752671.1:n.1312G>A (DGKE)
XR_001752672.1:n.1313G>A (DGKE)
XR_002958079.1:n.1311G>A (DGKE)
NM_003647.3:c.1147G>A (DGKE) MANE Select NP_003638.1:p.Ala383Thr