Canonical Allele Identifier: CA500687169

Gene: DGKE TRIM25

Linked Data

• dbSNP Id: rs1329968386
• gnomAD v2: 17-54926080-A-G
• gnomAD v3: 17-56848719-A-G
• gnomAD v4: 17-56848719-A-G
• MyVariant Identifiers: chr17:g.54926080A>G (hg19) ; chr17:g.56848719A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848719A>G , CM000679.2:g.56848719A>G	GRCh38
NC_000017.10:g.54926080A>G , CM000679.1:g.54926080A>G	GRCh37
NC_000017.9:g.52281079A>G	NCBI36
NG_033888.1:g.19621A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000284061.8:c.912A>G (DGKE) MANE Select	ENSP00000284061.3:p.Gln304=
ENST00000648772.1:c.*313+3224T>C (TRIM25)	ENSP00000498158.1:n.*313+3224T>C
ENST00000284061.7:c.912A>G (DGKE)	ENSP00000284061.3:p.Gln304=
ENST00000572944.1:c.742A>G (DGKE)
NM_003647.2:c.912A>G (DGKE)	NP_003638.1:p.Gln304=
XM_011525394.1:c.966A>G (DGKE)	XP_011523696.1:p.Gln322=
XM_011525395.1:c.966A>G (DGKE)	XP_011523697.1:p.Gln322=
XM_011525396.1:c.966A>G (DGKE)	XP_011523698.1:p.Gln322=
XM_011525397.1:c.966A>G (DGKE)	XP_011523699.1:p.Gln322=
XM_011525398.1:c.456A>G (DGKE)	XP_011523700.1:p.Gln152=
XR_934581.1:n.1065A>G (DGKE)
XM_011525394.3:c.966A>G (DGKE)	XP_011523696.1:p.Gln322=
XM_011525395.2:c.966A>G (DGKE)	XP_011523697.1:p.Gln322=
XM_011525396.2:c.966A>G (DGKE)	XP_011523698.1:p.Gln322=
XM_017025243.2:c.1284A>G (DGKE)	XP_016880732.1:p.Gln428=
XM_017025244.2:c.966A>G (DGKE)	XP_016880733.1:p.Gln322=
XR_001752670.2:n.1470A>G (DGKE)
XR_001752671.1:n.1077A>G (DGKE)
XR_001752672.1:n.1078A>G (DGKE)
XR_002958079.1:n.1076A>G (DGKE)
NM_003647.3:c.912A>G (DGKE) MANE Select	NP_003638.1:p.Gln304=