Canonical Allele Identifier: CA500686018

Gene: DGKE TRIM25

Linked Data

• gnomAD v4: 17-56845795-T-C
• MyVariant Identifiers: chr17:g.54923156T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56845795T>C , CM000679.2:g.56845795T>C	GRCh38
NC_000017.10:g.54923156T>C , CM000679.1:g.54923156T>C	GRCh37
NC_000017.9:g.52278155T>C	NCBI36
NG_033888.1:g.16697T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000284061.8:c.730T>C (DGKE) MANE Select	ENSP00000284061.3:p.Leu244=
ENST00000648772.1:c.*314-2005A>G (TRIM25)	ENSP00000498158.1:n.*314-2005A>G
ENST00000284061.7:c.730T>C (DGKE)	ENSP00000284061.3:p.Leu244=
ENST00000571084.1:n.266T>C (DGKE)
ENST00000572944.1:c.560T>C (DGKE)
ENST00000576869.5:n.878T>C (DGKE)
NM_003647.2:c.730T>C (DGKE)	NP_003638.1:p.Leu244=
XM_011525394.1:c.784T>C (DGKE)	XP_011523696.1:p.Leu262=
XM_011525395.1:c.784T>C (DGKE)	XP_011523697.1:p.Leu262=
XM_011525396.1:c.784T>C (DGKE)	XP_011523698.1:p.Leu262=
XM_011525397.1:c.784T>C (DGKE)	XP_011523699.1:p.Leu262=
XM_011525398.1:c.274T>C (DGKE)	XP_011523700.1:p.Leu92=
XR_934581.1:n.883T>C (DGKE)
XM_011525394.3:c.784T>C (DGKE)	XP_011523696.1:p.Leu262=
XM_011525395.2:c.784T>C (DGKE)	XP_011523697.1:p.Leu262=
XM_011525396.2:c.784T>C (DGKE)	XP_011523698.1:p.Leu262=
XM_017025243.2:c.730T>C (DGKE)	XP_016880732.1:p.Leu244=
XM_017025244.2:c.784T>C (DGKE)	XP_016880733.1:p.Leu262=
XR_001752670.2:n.916T>C (DGKE)
XR_001752671.1:n.895T>C (DGKE)
XR_001752672.1:n.896T>C (DGKE)
XR_002958079.1:n.894T>C (DGKE)
NM_003647.3:c.730T>C (DGKE) MANE Select	NP_003638.1:p.Leu244=