Canonical Allele Identifier: CA2266998702

Gene: TRIM25 DGKE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56856582G= , CM000679.2:g.56856582G=	GRCh38
NC_000017.10:g.54933943G= , CM000679.1:g.54933943G=	GRCh37
NC_000017.9:g.52288942G=	NCBI36
NG_033888.1:g.27484G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682766.1:c.1364-1472C= (TRIM25)	ENSP00000507876.1:n.1364-1472C=
ENST00000284061.8:c.1169G= (DGKE) MANE Select	ENSP00000284061.3:p.Arg390=
ENST00000648772.1:c.1364-1472C= (TRIM25)	ENSP00000498158.1:n.1364-1472C=
ENST00000284061.7:c.1169G= (DGKE)	ENSP00000284061.3:p.Arg390=
ENST00000572944.1:c.999G= (DGKE)
NM_003647.2:c.1169G= (DGKE)	NP_003638.1:p.Arg390=
XM_011525394.1:c.1223G= (DGKE)	XP_011523696.1:p.Arg408=
XM_011525395.1:c.1223G= (DGKE)	XP_011523697.1:p.Arg408=
XM_011525396.1:c.1223G= (DGKE)	XP_011523698.1:p.Arg408=
XM_011525397.1:c.1223G= (DGKE)	XP_011523699.1:p.Arg408=
XM_011525398.1:c.713G= (DGKE)	XP_011523700.1:p.Arg238=
XR_934581.1:n.1322G= (DGKE)
XM_011525394.3:c.1223G= (DGKE)	XP_011523696.1:p.Arg408=
XM_011525395.2:c.1223G= (DGKE)	XP_011523697.1:p.Arg408=
XM_011525396.2:c.1223G= (DGKE)	XP_011523698.1:p.Arg408=
XM_017025243.2:c.1541G= (DGKE)	XP_016880732.1:p.Arg514=
XM_017025244.2:c.1223G= (DGKE)	XP_016880733.1:p.Arg408=
XR_001752670.2:n.1727G= (DGKE)
XR_001752671.1:n.1334G= (DGKE)
XR_001752672.1:n.1335G= (DGKE)
XR_002958079.1:n.1333G= (DGKE)
NM_003647.3:c.1169G= (DGKE) MANE Select	NP_003638.1:p.Arg390=