Canonical Allele Identifier: CA399927854

Gene: DGKE TRIM25

Linked Data

• MyVariant Identifiers: chr17:g.54926112A>T (hg19) ; chr17:g.56848751A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848751A>T , CM000679.2:g.56848751A>T	GRCh38
NC_000017.10:g.54926112A>T , CM000679.1:g.54926112A>T	GRCh37
NC_000017.9:g.52281111A>T	NCBI36
NG_033888.1:g.19653A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000284061.8:c.944A>T (DGKE) MANE Select	ENSP00000284061.3:p.Asp315Val
ENST00000648772.1:c.*313+3192T>A (TRIM25)	ENSP00000498158.1:n.*313+3192T>A
ENST00000284061.7:c.944A>T (DGKE)	ENSP00000284061.3:p.Asp315Val
ENST00000572944.1:c.774A>T (DGKE)
NM_003647.2:c.944A>T (DGKE)	NP_003638.1:p.Asp315Val
XM_011525394.1:c.998A>T (DGKE)	XP_011523696.1:p.Asp333Val
XM_011525395.1:c.998A>T (DGKE)	XP_011523697.1:p.Asp333Val
XM_011525396.1:c.998A>T (DGKE)	XP_011523698.1:p.Asp333Val
XM_011525397.1:c.998A>T (DGKE)	XP_011523699.1:p.Asp333Val
XM_011525398.1:c.488A>T (DGKE)	XP_011523700.1:p.Asp163Val
XR_934581.1:n.1097A>T (DGKE)
XM_011525394.3:c.998A>T (DGKE)	XP_011523696.1:p.Asp333Val
XM_011525395.2:c.998A>T (DGKE)	XP_011523697.1:p.Asp333Val
XM_011525396.2:c.998A>T (DGKE)	XP_011523698.1:p.Asp333Val
XM_017025243.2:c.1316A>T (DGKE)	XP_016880732.1:p.Asp439Val
XM_017025244.2:c.998A>T (DGKE)	XP_016880733.1:p.Asp333Val
XR_001752670.2:n.1502A>T (DGKE)
XR_001752671.1:n.1109A>T (DGKE)
XR_001752672.1:n.1110A>T (DGKE)
XR_002958079.1:n.1108A>T (DGKE)
NM_003647.3:c.944A>T (DGKE) MANE Select	NP_003638.1:p.Asp315Val