Canonical Allele Identifier: CA500685942

Gene: DGKE TRIM25

Linked Data

• MyVariant Identifiers: chr17:g.54923089A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56845728A>C , CM000679.2:g.56845728A>C	GRCh38
NC_000017.10:g.54923089A>C , CM000679.1:g.54923089A>C	GRCh37
NC_000017.9:g.52278088A>C	NCBI36
NG_033888.1:g.16630A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.663A>C (DGKE) MANE Select	ENSP00000284061.3:p.Ile221=
ENST00000648772.1:c.*314-1938T>G (TRIM25)	ENSP00000498158.1:n.*314-1938T>G
ENST00000284061.7:c.663A>C (DGKE)	ENSP00000284061.3:p.Ile221=
ENST00000571084.1:n.199A>C (DGKE)
ENST00000572944.1:c.493A>C (DGKE)
ENST00000576869.5:n.811A>C (DGKE)
NM_003647.2:c.663A>C (DGKE)	NP_003638.1:p.Ile221=
XM_011525394.1:c.717A>C (DGKE)	XP_011523696.1:p.Ile239=
XM_011525395.1:c.717A>C (DGKE)	XP_011523697.1:p.Ile239=
XM_011525396.1:c.717A>C (DGKE)	XP_011523698.1:p.Ile239=
XM_011525397.1:c.717A>C (DGKE)	XP_011523699.1:p.Ile239=
XM_011525398.1:c.207A>C (DGKE)	XP_011523700.1:p.Ile69=
XR_934581.1:n.816A>C (DGKE)
XM_011525394.3:c.717A>C (DGKE)	XP_011523696.1:p.Ile239=
XM_011525395.2:c.717A>C (DGKE)	XP_011523697.1:p.Ile239=
XM_011525396.2:c.717A>C (DGKE)	XP_011523698.1:p.Ile239=
XM_017025243.2:c.663A>C (DGKE)	XP_016880732.1:p.Ile221=
XM_017025244.2:c.717A>C (DGKE)	XP_016880733.1:p.Ile239=
XR_001752670.2:n.849A>C (DGKE)
XR_001752671.1:n.828A>C (DGKE)
XR_001752672.1:n.829A>C (DGKE)
XR_002958079.1:n.827A>C (DGKE)
NM_003647.3:c.663A>C (DGKE) MANE Select	NP_003638.1:p.Ile221=