Canonical Allele Identifier: CA2266993764

Gene: DGKE TRIM25

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56845932G= , CM000679.2:g.56845932G=	GRCh38
NC_000017.10:g.54923293G= , CM000679.1:g.54923293G=	GRCh37
NC_000017.9:g.52278292G=	NCBI36
NG_033888.1:g.16834G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.744+123G= (DGKE) MANE Select	ENSP00000284061.3:n.744+123G=
ENST00000648772.1:c.*314-2142C= (TRIM25)	ENSP00000498158.1:n.*314-2142C=
ENST00000284061.7:c.744+123G= (DGKE)	ENSP00000284061.3:n.744+123G=
ENST00000571084.1:n.403G= (DGKE)
ENST00000572944.1:c.574+123G= (DGKE)
ENST00000576869.5:n.892+123G= (DGKE)
NM_003647.2:c.744+123G= (DGKE)	NP_003638.1:n.744+123G=
XM_011525394.1:c.798+123G= (DGKE)	XP_011523696.1:n.798+123G=
XM_011525395.1:c.798+123G= (DGKE)	XP_011523697.1:n.798+123G=
XM_011525396.1:c.798+123G= (DGKE)	XP_011523698.1:n.798+123G=
XM_011525397.1:c.798+123G= (DGKE)	XP_011523699.1:n.798+123G=
XM_011525398.1:c.288+123G= (DGKE)	XP_011523700.1:n.288+123G=
XR_934581.1:n.897+123G= (DGKE)
XM_011525394.3:c.798+123G= (DGKE)	XP_011523696.1:n.798+123G=
XM_011525395.2:c.798+123G= (DGKE)	XP_011523697.1:n.798+123G=
XM_011525396.2:c.798+123G= (DGKE)	XP_011523698.1:n.798+123G=
XM_017025243.2:c.744+123G= (DGKE)	XP_016880732.1:n.744+123G=
XM_017025244.2:c.798+123G= (DGKE)	XP_016880733.1:n.798+123G=
XR_001752670.2:n.930+123G= (DGKE)
XR_001752671.1:n.909+123G= (DGKE)
XR_001752672.1:n.910+123G= (DGKE)
XR_002958079.1:n.908+123G= (DGKE)
NM_003647.3:c.744+123G= (DGKE) MANE Select	NP_003638.1:n.744+123G=