Canonical Allele Identifier: CA399926674

Gene: DGKE TRIM25

Linked Data

• dbSNP Id: rs1210748351
• gnomAD v2: 17-54923067-G-T
• gnomAD v4: 17-56845706-G-T
• MyVariant Identifiers: chr17:g.54923067G>T (hg19) ; chr17:g.56845706G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56845706G>T , CM000679.2:g.56845706G>T	GRCh38
NC_000017.10:g.54923067G>T , CM000679.1:g.54923067G>T	GRCh37
NC_000017.9:g.52278066G>T	NCBI36
NG_033888.1:g.16608G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000284061.8:c.641G>T (DGKE) MANE Select	ENSP00000284061.3:p.Gly214Val
ENST00000648772.1:c.*314-1916C>A (TRIM25)	ENSP00000498158.1:n.*314-1916C>A
ENST00000284061.7:c.641G>T (DGKE)	ENSP00000284061.3:p.Gly214Val
ENST00000571084.1:n.177G>T (DGKE)
ENST00000572944.1:c.471G>T (DGKE)
ENST00000576869.5:n.789G>T (DGKE)
NM_003647.2:c.641G>T (DGKE)	NP_003638.1:p.Gly214Val
XM_011525394.1:c.695G>T (DGKE)	XP_011523696.1:p.Gly232Val
XM_011525395.1:c.695G>T (DGKE)	XP_011523697.1:p.Gly232Val
XM_011525396.1:c.695G>T (DGKE)	XP_011523698.1:p.Gly232Val
XM_011525397.1:c.695G>T (DGKE)	XP_011523699.1:p.Gly232Val
XM_011525398.1:c.185G>T (DGKE)	XP_011523700.1:p.Gly62Val
XR_934581.1:n.794G>T (DGKE)
XM_011525394.3:c.695G>T (DGKE)	XP_011523696.1:p.Gly232Val
XM_011525395.2:c.695G>T (DGKE)	XP_011523697.1:p.Gly232Val
XM_011525396.2:c.695G>T (DGKE)	XP_011523698.1:p.Gly232Val
XM_017025243.2:c.641G>T (DGKE)	XP_016880732.1:p.Gly214Val
XM_017025244.2:c.695G>T (DGKE)	XP_016880733.1:p.Gly232Val
XR_001752670.2:n.827G>T (DGKE)
XR_001752671.1:n.806G>T (DGKE)
XR_001752672.1:n.807G>T (DGKE)
XR_002958079.1:n.805G>T (DGKE)
NM_003647.3:c.641G>T (DGKE) MANE Select	NP_003638.1:p.Gly214Val