Canonical Allele Identifier: CA500685932

Gene: DGKE TRIM25

Linked Data

• MyVariant Identifiers: chr17:g.54923068A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56845707A>G , CM000679.2:g.56845707A>G	GRCh38
NC_000017.10:g.54923068A>G , CM000679.1:g.54923068A>G	GRCh37
NC_000017.9:g.52278067A>G	NCBI36
NG_033888.1:g.16609A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.642A>G (DGKE) MANE Select	ENSP00000284061.3:p.Gly214=
ENST00000648772.1:c.*314-1917T>C (TRIM25)	ENSP00000498158.1:n.*314-1917T>C
ENST00000284061.7:c.642A>G (DGKE)	ENSP00000284061.3:p.Gly214=
ENST00000571084.1:n.178A>G (DGKE)
ENST00000572944.1:c.472A>G (DGKE)
ENST00000576869.5:n.790A>G (DGKE)
NM_003647.2:c.642A>G (DGKE)	NP_003638.1:p.Gly214=
XM_011525394.1:c.696A>G (DGKE)	XP_011523696.1:p.Gly232=
XM_011525395.1:c.696A>G (DGKE)	XP_011523697.1:p.Gly232=
XM_011525396.1:c.696A>G (DGKE)	XP_011523698.1:p.Gly232=
XM_011525397.1:c.696A>G (DGKE)	XP_011523699.1:p.Gly232=
XM_011525398.1:c.186A>G (DGKE)	XP_011523700.1:p.Gly62=
XR_934581.1:n.795A>G (DGKE)
XM_011525394.3:c.696A>G (DGKE)	XP_011523696.1:p.Gly232=
XM_011525395.2:c.696A>G (DGKE)	XP_011523697.1:p.Gly232=
XM_011525396.2:c.696A>G (DGKE)	XP_011523698.1:p.Gly232=
XM_017025243.2:c.642A>G (DGKE)	XP_016880732.1:p.Gly214=
XM_017025244.2:c.696A>G (DGKE)	XP_016880733.1:p.Gly232=
XR_001752670.2:n.828A>G (DGKE)
XR_001752671.1:n.807A>G (DGKE)
XR_001752672.1:n.808A>G (DGKE)
XR_002958079.1:n.806A>G (DGKE)
NM_003647.3:c.642A>G (DGKE) MANE Select	NP_003638.1:p.Gly214=