Canonical Allele Identifier: CA2266993800

Gene: DGKE TRIM25

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56846000C= , CM000679.2:g.56846000C=	GRCh38
NC_000017.10:g.54923361C= , CM000679.1:g.54923361C=	GRCh37
NC_000017.9:g.52278360C=	NCBI36
NG_033888.1:g.16902C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.744+191C= (DGKE) MANE Select	ENSP00000284061.3:n.744+191C=
ENST00000648772.1:c.*314-2210G= (TRIM25)	ENSP00000498158.1:n.*314-2210G=
ENST00000284061.7:c.744+191C= (DGKE)	ENSP00000284061.3:n.744+191C=
ENST00000571084.1:n.471C= (DGKE)
ENST00000572944.1:c.574+191C= (DGKE)
ENST00000576869.5:n.892+191C= (DGKE)
NM_003647.2:c.744+191C= (DGKE)	NP_003638.1:n.744+191C=
XM_011525394.1:c.798+191C= (DGKE)	XP_011523696.1:n.798+191C=
XM_011525395.1:c.798+191C= (DGKE)	XP_011523697.1:n.798+191C=
XM_011525396.1:c.798+191C= (DGKE)	XP_011523698.1:n.798+191C=
XM_011525397.1:c.798+191C= (DGKE)	XP_011523699.1:n.798+191C=
XM_011525398.1:c.288+191C= (DGKE)	XP_011523700.1:n.288+191C=
XR_934581.1:n.897+191C= (DGKE)
XM_011525394.3:c.798+191C= (DGKE)	XP_011523696.1:n.798+191C=
XM_011525395.2:c.798+191C= (DGKE)	XP_011523697.1:n.798+191C=
XM_011525396.2:c.798+191C= (DGKE)	XP_011523698.1:n.798+191C=
XM_017025243.2:c.744+191C= (DGKE)	XP_016880732.1:n.744+191C=
XM_017025244.2:c.798+191C= (DGKE)	XP_016880733.1:n.798+191C=
XR_001752670.2:n.930+191C= (DGKE)
XR_001752671.1:n.909+191C= (DGKE)
XR_001752672.1:n.910+191C= (DGKE)
XR_002958079.1:n.908+191C= (DGKE)
NM_003647.3:c.744+191C= (DGKE) MANE Select	NP_003638.1:n.744+191C=