Canonical Allele Identifier: CA399927742

Gene: DGKE TRIM25

Linked Data

• MyVariant Identifiers: chr17:g.54926078C>T (hg19) ; chr17:g.56848717C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848717C>T , CM000679.2:g.56848717C>T	GRCh38
NC_000017.10:g.54926078C>T , CM000679.1:g.54926078C>T	GRCh37
NC_000017.9:g.52281077C>T	NCBI36
NG_033888.1:g.19619C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000284061.8:c.910C>T (DGKE) MANE Select	ENSP00000284061.3:p.Gln304Ter
ENST00000648772.1:c.*313+3226G>A (TRIM25)	ENSP00000498158.1:n.*313+3226G>A
ENST00000284061.7:c.910C>T (DGKE)	ENSP00000284061.3:p.Gln304Ter
ENST00000572944.1:c.740C>T (DGKE)
NM_003647.2:c.910C>T (DGKE)	NP_003638.1:p.Gln304Ter
XM_011525394.1:c.964C>T (DGKE)	XP_011523696.1:p.Gln322Ter
XM_011525395.1:c.964C>T (DGKE)	XP_011523697.1:p.Gln322Ter
XM_011525396.1:c.964C>T (DGKE)	XP_011523698.1:p.Gln322Ter
XM_011525397.1:c.964C>T (DGKE)	XP_011523699.1:p.Gln322Ter
XM_011525398.1:c.454C>T (DGKE)	XP_011523700.1:p.Gln152Ter
XR_934581.1:n.1063C>T (DGKE)
XM_011525394.3:c.964C>T (DGKE)	XP_011523696.1:p.Gln322Ter
XM_011525395.2:c.964C>T (DGKE)	XP_011523697.1:p.Gln322Ter
XM_011525396.2:c.964C>T (DGKE)	XP_011523698.1:p.Gln322Ter
XM_017025243.2:c.1282C>T (DGKE)	XP_016880732.1:p.Gln428Ter
XM_017025244.2:c.964C>T (DGKE)	XP_016880733.1:p.Gln322Ter
XR_001752670.2:n.1468C>T (DGKE)
XR_001752671.1:n.1075C>T (DGKE)
XR_001752672.1:n.1076C>T (DGKE)
XR_002958079.1:n.1074C>T (DGKE)
NM_003647.3:c.910C>T (DGKE) MANE Select	NP_003638.1:p.Gln304Ter