Canonical Allele Identifier: CA500664669

Gene: TRIM25 DGKE

Linked Data

• MyVariant Identifiers: chr17:g.54933932T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56856571T>C , CM000679.2:g.56856571T>C	GRCh38
NC_000017.10:g.54933932T>C , CM000679.1:g.54933932T>C	GRCh37
NC_000017.9:g.52288931T>C	NCBI36
NG_033888.1:g.27473T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682766.1:c.1364-1461A>G (TRIM25)	ENSP00000507876.1:n.1364-1461A>G
ENST00000284061.8:c.1158T>C (DGKE) MANE Select	ENSP00000284061.3:p.Phe386=
ENST00000648772.1:c.1364-1461A>G (TRIM25)	ENSP00000498158.1:n.1364-1461A>G
ENST00000284061.7:c.1158T>C (DGKE)	ENSP00000284061.3:p.Phe386=
ENST00000572944.1:c.988T>C (DGKE)
NM_003647.2:c.1158T>C (DGKE)	NP_003638.1:p.Phe386=
XM_011525394.1:c.1212T>C (DGKE)	XP_011523696.1:p.Phe404=
XM_011525395.1:c.1212T>C (DGKE)	XP_011523697.1:p.Phe404=
XM_011525396.1:c.1212T>C (DGKE)	XP_011523698.1:p.Phe404=
XM_011525397.1:c.1212T>C (DGKE)	XP_011523699.1:p.Phe404=
XM_011525398.1:c.702T>C (DGKE)	XP_011523700.1:p.Phe234=
XR_934581.1:n.1311T>C (DGKE)
XM_011525394.3:c.1212T>C (DGKE)	XP_011523696.1:p.Phe404=
XM_011525395.2:c.1212T>C (DGKE)	XP_011523697.1:p.Phe404=
XM_011525396.2:c.1212T>C (DGKE)	XP_011523698.1:p.Phe404=
XM_017025243.2:c.1530T>C (DGKE)	XP_016880732.1:p.Phe510=
XM_017025244.2:c.1212T>C (DGKE)	XP_016880733.1:p.Phe404=
XR_001752670.2:n.1716T>C (DGKE)
XR_001752671.1:n.1323T>C (DGKE)
XR_001752672.1:n.1324T>C (DGKE)
XR_002958079.1:n.1322T>C (DGKE)
NM_003647.3:c.1158T>C (DGKE) MANE Select	NP_003638.1:p.Phe386=