Canonical Allele Identifier: CA500664715

Gene: TRIM25 DGKE

Linked Data

• MyVariant Identifiers: chr17:g.54933938T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56856577T>A , CM000679.2:g.56856577T>A	GRCh38
NC_000017.10:g.54933938T>A , CM000679.1:g.54933938T>A	GRCh37
NC_000017.9:g.52288937T>A	NCBI36
NG_033888.1:g.27479T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682766.1:c.1364-1467A>T (TRIM25)	ENSP00000507876.1:n.1364-1467A>T
ENST00000284061.8:c.1164T>A (DGKE) MANE Select	ENSP00000284061.3:p.Ala388=
ENST00000648772.1:c.1364-1467A>T (TRIM25)	ENSP00000498158.1:n.1364-1467A>T
ENST00000284061.7:c.1164T>A (DGKE)	ENSP00000284061.3:p.Ala388=
ENST00000572944.1:c.994T>A (DGKE)
NM_003647.2:c.1164T>A (DGKE)	NP_003638.1:p.Ala388=
XM_011525394.1:c.1218T>A (DGKE)	XP_011523696.1:p.Ala406=
XM_011525395.1:c.1218T>A (DGKE)	XP_011523697.1:p.Ala406=
XM_011525396.1:c.1218T>A (DGKE)	XP_011523698.1:p.Ala406=
XM_011525397.1:c.1218T>A (DGKE)	XP_011523699.1:p.Ala406=
XM_011525398.1:c.708T>A (DGKE)	XP_011523700.1:p.Ala236=
XR_934581.1:n.1317T>A (DGKE)
XM_011525394.3:c.1218T>A (DGKE)	XP_011523696.1:p.Ala406=
XM_011525395.2:c.1218T>A (DGKE)	XP_011523697.1:p.Ala406=
XM_011525396.2:c.1218T>A (DGKE)	XP_011523698.1:p.Ala406=
XM_017025243.2:c.1536T>A (DGKE)	XP_016880732.1:p.Ala512=
XM_017025244.2:c.1218T>A (DGKE)	XP_016880733.1:p.Ala406=
XR_001752670.2:n.1722T>A (DGKE)
XR_001752671.1:n.1329T>A (DGKE)
XR_001752672.1:n.1330T>A (DGKE)
XR_002958079.1:n.1328T>A (DGKE)
NM_003647.3:c.1164T>A (DGKE) MANE Select	NP_003638.1:p.Ala388=