Canonical Allele Identifier: CA500687388

Gene: DGKE TRIM25

Linked Data

• gnomAD v4: 17-56848812-T-G
• MyVariant Identifiers: chr17:g.54926173T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848812T>G , CM000679.2:g.56848812T>G	GRCh38
NC_000017.10:g.54926173T>G , CM000679.1:g.54926173T>G	GRCh37
NC_000017.9:g.52281172T>G	NCBI36
NG_033888.1:g.19714T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.1005T>G (DGKE) MANE Select	ENSP00000284061.3:p.Val335=
ENST00000648772.1:c.*313+3131A>C (TRIM25)	ENSP00000498158.1:n.*313+3131A>C
ENST00000284061.7:c.1005T>G (DGKE)	ENSP00000284061.3:p.Val335=
ENST00000572944.1:c.835T>G (DGKE)
NM_003647.2:c.1005T>G (DGKE)	NP_003638.1:p.Val335=
XM_011525394.1:c.1059T>G (DGKE)	XP_011523696.1:p.Val353=
XM_011525395.1:c.1059T>G (DGKE)	XP_011523697.1:p.Val353=
XM_011525396.1:c.1059T>G (DGKE)	XP_011523698.1:p.Val353=
XM_011525397.1:c.1059T>G (DGKE)	XP_011523699.1:p.Val353=
XM_011525398.1:c.549T>G (DGKE)	XP_011523700.1:p.Val183=
XR_934581.1:n.1158T>G (DGKE)
XM_011525394.3:c.1059T>G (DGKE)	XP_011523696.1:p.Val353=
XM_011525395.2:c.1059T>G (DGKE)	XP_011523697.1:p.Val353=
XM_011525396.2:c.1059T>G (DGKE)	XP_011523698.1:p.Val353=
XM_017025243.2:c.1377T>G (DGKE)	XP_016880732.1:p.Val459=
XM_017025244.2:c.1059T>G (DGKE)	XP_016880733.1:p.Val353=
XR_001752670.2:n.1563T>G (DGKE)
XR_001752671.1:n.1170T>G (DGKE)
XR_001752672.1:n.1171T>G (DGKE)
XR_002958079.1:n.1169T>G (DGKE)
NM_003647.3:c.1005T>G (DGKE) MANE Select	NP_003638.1:p.Val335=