Canonical Allele Identifier: CA2266995169

Gene: DGKE TRIM25

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848891T= , CM000679.2:g.56848891T=	GRCh38
NC_000017.10:g.54926252T= , CM000679.1:g.54926252T=	GRCh37
NC_000017.9:g.52281251T=	NCBI36
NG_033888.1:g.19793T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.1046+38T= (DGKE) MANE Select	ENSP00000284061.3:n.1046+38T=
ENST00000648772.1:c.*313+3052A= (TRIM25)	ENSP00000498158.1:n.*313+3052A=
ENST00000284061.7:c.1046+38T= (DGKE)	ENSP00000284061.3:n.1046+38T=
ENST00000572944.1:c.876+38T= (DGKE)
NM_003647.2:c.1046+38T= (DGKE)	NP_003638.1:n.1046+38T=
XM_011525394.1:c.1100+38T= (DGKE)	XP_011523696.1:n.1100+38T=
XM_011525395.1:c.1100+38T= (DGKE)	XP_011523697.1:n.1100+38T=
XM_011525396.1:c.1100+38T= (DGKE)	XP_011523698.1:n.1100+38T=
XM_011525397.1:c.1100+38T= (DGKE)	XP_011523699.1:n.1100+38T=
XM_011525398.1:c.590+38T= (DGKE)	XP_011523700.1:n.590+38T=
XR_934581.1:n.1199+38T= (DGKE)
XM_011525394.3:c.1100+38T= (DGKE)	XP_011523696.1:n.1100+38T=
XM_011525395.2:c.1100+38T= (DGKE)	XP_011523697.1:n.1100+38T=
XM_011525396.2:c.1100+38T= (DGKE)	XP_011523698.1:n.1100+38T=
XM_017025243.2:c.1418+38T= (DGKE)	XP_016880732.1:n.1418+38T=
XM_017025244.2:c.1100+38T= (DGKE)	XP_016880733.1:n.1100+38T=
XR_001752670.2:n.1604+38T= (DGKE)
XR_001752671.1:n.1211+38T= (DGKE)
XR_001752672.1:n.1212+38T= (DGKE)
XR_002958079.1:n.1210+38T= (DGKE)
NM_003647.3:c.1046+38T= (DGKE) MANE Select	NP_003638.1:n.1046+38T=