Canonical Allele Identifier: CA2266995020

Gene: DGKE TRIM25

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848528G= , CM000679.2:g.56848528G=	GRCh38
NC_000017.10:g.54925889G= , CM000679.1:g.54925889G=	GRCh37
NC_000017.9:g.52280888G=	NCBI36
NG_033888.1:g.19430G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000284061.8:c.889-168G= (DGKE) MANE Select	ENSP00000284061.3:n.889-168G=
ENST00000648772.1:c.*313+3415C= (TRIM25)	ENSP00000498158.1:n.*313+3415C=
ENST00000284061.7:c.889-168G= (DGKE)	ENSP00000284061.3:n.889-168G=
ENST00000572944.1:c.719-168G= (DGKE)
NM_003647.2:c.889-168G= (DGKE)	NP_003638.1:n.889-168G=
XM_011525394.1:c.943-168G= (DGKE)	XP_011523696.1:n.943-168G=
XM_011525395.1:c.943-168G= (DGKE)	XP_011523697.1:n.943-168G=
XM_011525396.1:c.943-168G= (DGKE)	XP_011523698.1:n.943-168G=
XM_011525397.1:c.943-168G= (DGKE)	XP_011523699.1:n.943-168G=
XM_011525398.1:c.433-168G= (DGKE)	XP_011523700.1:n.433-168G=
XR_934581.1:n.1042-168G= (DGKE)
XM_011525394.3:c.943-168G= (DGKE)	XP_011523696.1:n.943-168G=
XM_011525395.2:c.943-168G= (DGKE)	XP_011523697.1:n.943-168G=
XM_011525396.2:c.943-168G= (DGKE)	XP_011523698.1:n.943-168G=
XM_017025243.2:c.1260+91G= (DGKE)	XP_016880732.1:n.1260+91G=
XM_017025244.2:c.943-168G= (DGKE)	XP_016880733.1:n.943-168G=
XR_001752670.2:n.1446+91G= (DGKE)
XR_001752671.1:n.1054-168G= (DGKE)
XR_001752672.1:n.1055-168G= (DGKE)
XR_002958079.1:n.1053-168G= (DGKE)
NM_003647.3:c.889-168G= (DGKE) MANE Select	NP_003638.1:n.889-168G=