Canonical Allele Identifier: CA2266995177

Gene: DGKE TRIM25

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848904G= , CM000679.2:g.56848904G=	GRCh38
NC_000017.10:g.54926265G= , CM000679.1:g.54926265G=	GRCh37
NC_000017.9:g.52281264G=	NCBI36
NG_033888.1:g.19806G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.1046+51G= (DGKE) MANE Select	ENSP00000284061.3:n.1046+51G=
ENST00000648772.1:c.*313+3039C= (TRIM25)	ENSP00000498158.1:n.*313+3039C=
ENST00000284061.7:c.1046+51G= (DGKE)	ENSP00000284061.3:n.1046+51G=
ENST00000572944.1:c.876+51G= (DGKE)
NM_003647.2:c.1046+51G= (DGKE)	NP_003638.1:n.1046+51G=
XM_011525394.1:c.1100+51G= (DGKE)	XP_011523696.1:n.1100+51G=
XM_011525395.1:c.1100+51G= (DGKE)	XP_011523697.1:n.1100+51G=
XM_011525396.1:c.1100+51G= (DGKE)	XP_011523698.1:n.1100+51G=
XM_011525397.1:c.1100+51G= (DGKE)	XP_011523699.1:n.1100+51G=
XM_011525398.1:c.590+51G= (DGKE)	XP_011523700.1:n.590+51G=
XR_934581.1:n.1199+51G= (DGKE)
XM_011525394.3:c.1100+51G= (DGKE)	XP_011523696.1:n.1100+51G=
XM_011525395.2:c.1100+51G= (DGKE)	XP_011523697.1:n.1100+51G=
XM_011525396.2:c.1100+51G= (DGKE)	XP_011523698.1:n.1100+51G=
XM_017025243.2:c.1418+51G= (DGKE)	XP_016880732.1:n.1418+51G=
XM_017025244.2:c.1100+51G= (DGKE)	XP_016880733.1:n.1100+51G=
XR_001752670.2:n.1604+51G= (DGKE)
XR_001752671.1:n.1211+51G= (DGKE)
XR_001752672.1:n.1212+51G= (DGKE)
XR_002958079.1:n.1210+51G= (DGKE)
NM_003647.3:c.1046+51G= (DGKE) MANE Select	NP_003638.1:n.1046+51G=