Canonical Allele Identifier: CA399927914

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848780G>A , CM000679.2:g.56848780G>A GRCh38
NC_000017.10:g.54926141G>A , CM000679.1:g.54926141G>A GRCh37
NC_000017.9:g.52281140G>A NCBI36
NG_033888.1:g.19682G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.973G>A (DGKE) MANE Select ENSP00000284061.3:p.Gly325Ser
ENST00000648772.1:c.*313+3163C>T (TRIM25) ENSP00000498158.1:n.*313+3163C>T
ENST00000284061.7:c.973G>A (DGKE) ENSP00000284061.3:p.Gly325Ser
ENST00000572944.1:c.803G>A (DGKE)
NM_003647.2:c.973G>A (DGKE) NP_003638.1:p.Gly325Ser
XM_011525394.1:c.1027G>A (DGKE) XP_011523696.1:p.Gly343Ser
XM_011525395.1:c.1027G>A (DGKE) XP_011523697.1:p.Gly343Ser
XM_011525396.1:c.1027G>A (DGKE) XP_011523698.1:p.Gly343Ser
XM_011525397.1:c.1027G>A (DGKE) XP_011523699.1:p.Gly343Ser
XM_011525398.1:c.517G>A (DGKE) XP_011523700.1:p.Gly173Ser
XR_934581.1:n.1126G>A (DGKE)
XM_011525394.3:c.1027G>A (DGKE) XP_011523696.1:p.Gly343Ser
XM_011525395.2:c.1027G>A (DGKE) XP_011523697.1:p.Gly343Ser
XM_011525396.2:c.1027G>A (DGKE) XP_011523698.1:p.Gly343Ser
XM_017025243.2:c.1345G>A (DGKE) XP_016880732.1:p.Gly449Ser
XM_017025244.2:c.1027G>A (DGKE) XP_016880733.1:p.Gly343Ser
XR_001752670.2:n.1531G>A (DGKE)
XR_001752671.1:n.1138G>A (DGKE)
XR_001752672.1:n.1139G>A (DGKE)
XR_002958079.1:n.1137G>A (DGKE)
NM_003647.3:c.973G>A (DGKE) MANE Select NP_003638.1:p.Gly325Ser