Canonical Allele Identifier: CA2266995124

Gene: DGKE TRIM25

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848805C= , CM000679.2:g.56848805C=	GRCh38
NC_000017.10:g.54926166C= , CM000679.1:g.54926166C=	GRCh37
NC_000017.9:g.52281165C=	NCBI36
NG_033888.1:g.19707C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.998C= (DGKE) MANE Select	ENSP00000284061.3:p.Ala333=
ENST00000648772.1:c.*313+3138G= (TRIM25)	ENSP00000498158.1:n.*313+3138G=
ENST00000284061.7:c.998C= (DGKE)	ENSP00000284061.3:p.Ala333=
ENST00000572944.1:c.828C= (DGKE)
NM_003647.2:c.998C= (DGKE)	NP_003638.1:p.Ala333=
XM_011525394.1:c.1052C= (DGKE)	XP_011523696.1:p.Ala351=
XM_011525395.1:c.1052C= (DGKE)	XP_011523697.1:p.Ala351=
XM_011525396.1:c.1052C= (DGKE)	XP_011523698.1:p.Ala351=
XM_011525397.1:c.1052C= (DGKE)	XP_011523699.1:p.Ala351=
XM_011525398.1:c.542C= (DGKE)	XP_011523700.1:p.Ala181=
XR_934581.1:n.1151C= (DGKE)
XM_011525394.3:c.1052C= (DGKE)	XP_011523696.1:p.Ala351=
XM_011525395.2:c.1052C= (DGKE)	XP_011523697.1:p.Ala351=
XM_011525396.2:c.1052C= (DGKE)	XP_011523698.1:p.Ala351=
XM_017025243.2:c.1370C= (DGKE)	XP_016880732.1:p.Ala457=
XM_017025244.2:c.1052C= (DGKE)	XP_016880733.1:p.Ala351=
XR_001752670.2:n.1556C= (DGKE)
XR_001752671.1:n.1163C= (DGKE)
XR_001752672.1:n.1164C= (DGKE)
XR_002958079.1:n.1162C= (DGKE)
NM_003647.3:c.998C= (DGKE) MANE Select	NP_003638.1:p.Ala333=