Canonical Allele Identifier: CA500685568

Gene: DGKE TRIM25

Linked Data

• MyVariant Identifiers: chr17:g.54921407T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56844046T>C , CM000679.2:g.56844046T>C	GRCh38
NC_000017.10:g.54921407T>C , CM000679.1:g.54921407T>C	GRCh37
NC_000017.9:g.52276406T>C	NCBI36
NG_033888.1:g.14948T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000284061.8:c.492T>C (DGKE) MANE Select	ENSP00000284061.3:p.His164=
ENST00000648772.1:c.*314-256A>G (TRIM25)	ENSP00000498158.1:n.*314-256A>G
ENST00000284061.7:c.492T>C (DGKE)	ENSP00000284061.3:p.His164=
ENST00000571084.1:n.28T>C (DGKE)
ENST00000572944.1:c.322T>C (DGKE)
ENST00000576869.5:n.640T>C (DGKE)
NM_003647.2:c.492T>C (DGKE)	NP_003638.1:p.His164=
XM_011525394.1:c.546T>C (DGKE)	XP_011523696.1:p.His182=
XM_011525395.1:c.546T>C (DGKE)	XP_011523697.1:p.His182=
XM_011525396.1:c.546T>C (DGKE)	XP_011523698.1:p.His182=
XM_011525397.1:c.546T>C (DGKE)	XP_011523699.1:p.His182=
XM_011525398.1:c.36T>C (DGKE)	XP_011523700.1:p.His12=
XR_934581.1:n.645T>C (DGKE)
XM_011525394.3:c.546T>C (DGKE)	XP_011523696.1:p.His182=
XM_011525395.2:c.546T>C (DGKE)	XP_011523697.1:p.His182=
XM_011525396.2:c.546T>C (DGKE)	XP_011523698.1:p.His182=
XM_017025243.2:c.492T>C (DGKE)	XP_016880732.1:p.His164=
XM_017025244.2:c.546T>C (DGKE)	XP_016880733.1:p.His182=
XR_001752670.2:n.678T>C (DGKE)
XR_001752671.1:n.657T>C (DGKE)
XR_001752672.1:n.658T>C (DGKE)
XR_002958079.1:n.656T>C (DGKE)
NM_003647.3:c.492T>C (DGKE) MANE Select	NP_003638.1:p.His164=