Canonical Allele Identifier: CA2266995096

Gene: DGKE TRIM25

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848714C= , CM000679.2:g.56848714C=	GRCh38
NC_000017.10:g.54926075C= , CM000679.1:g.54926075C=	GRCh37
NC_000017.9:g.52281074C=	NCBI36
NG_033888.1:g.19616C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000284061.8:c.907C= (DGKE) MANE Select	ENSP00000284061.3:p.Pro303=
ENST00000648772.1:c.*313+3229G= (TRIM25)	ENSP00000498158.1:n.*313+3229G=
ENST00000284061.7:c.907C= (DGKE)	ENSP00000284061.3:p.Pro303=
ENST00000572944.1:c.737C= (DGKE)
NM_003647.2:c.907C= (DGKE)	NP_003638.1:p.Pro303=
XM_011525394.1:c.961C= (DGKE)	XP_011523696.1:p.Pro321=
XM_011525395.1:c.961C= (DGKE)	XP_011523697.1:p.Pro321=
XM_011525396.1:c.961C= (DGKE)	XP_011523698.1:p.Pro321=
XM_011525397.1:c.961C= (DGKE)	XP_011523699.1:p.Pro321=
XM_011525398.1:c.451C= (DGKE)	XP_011523700.1:p.Pro151=
XR_934581.1:n.1060C= (DGKE)
XM_011525394.3:c.961C= (DGKE)	XP_011523696.1:p.Pro321=
XM_011525395.2:c.961C= (DGKE)	XP_011523697.1:p.Pro321=
XM_011525396.2:c.961C= (DGKE)	XP_011523698.1:p.Pro321=
XM_017025243.2:c.1279C= (DGKE)	XP_016880732.1:p.Pro427=
XM_017025244.2:c.961C= (DGKE)	XP_016880733.1:p.Pro321=
XR_001752670.2:n.1465C= (DGKE)
XR_001752671.1:n.1072C= (DGKE)
XR_001752672.1:n.1073C= (DGKE)
XR_002958079.1:n.1071C= (DGKE)
NM_003647.3:c.907C= (DGKE) MANE Select	NP_003638.1:p.Pro303=