Canonical Allele Identifier: CA500664301

Gene: TRIM25 DGKE

Linked Data

• MyVariant Identifiers: chr17:g.54933878C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56856517C>T , CM000679.2:g.56856517C>T	GRCh38
NC_000017.10:g.54933878C>T , CM000679.1:g.54933878C>T	GRCh37
NC_000017.9:g.52288877C>T	NCBI36
NG_033888.1:g.27419C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682766.1:c.1364-1407G>A (TRIM25)	ENSP00000507876.1:n.1364-1407G>A
ENST00000284061.8:c.1104C>T (DGKE) MANE Select	ENSP00000284061.3:p.Phe368=
ENST00000648772.1:c.1364-1407G>A (TRIM25)	ENSP00000498158.1:n.1364-1407G>A
ENST00000284061.7:c.1104C>T (DGKE)	ENSP00000284061.3:p.Phe368=
ENST00000572944.1:c.934C>T (DGKE)
NM_003647.2:c.1104C>T (DGKE)	NP_003638.1:p.Phe368=
XM_011525394.1:c.1158C>T (DGKE)	XP_011523696.1:p.Phe386=
XM_011525395.1:c.1158C>T (DGKE)	XP_011523697.1:p.Phe386=
XM_011525396.1:c.1158C>T (DGKE)	XP_011523698.1:p.Phe386=
XM_011525397.1:c.1158C>T (DGKE)	XP_011523699.1:p.Phe386=
XM_011525398.1:c.648C>T (DGKE)	XP_011523700.1:p.Phe216=
XR_934581.1:n.1257C>T (DGKE)
XM_011525394.3:c.1158C>T (DGKE)	XP_011523696.1:p.Phe386=
XM_011525395.2:c.1158C>T (DGKE)	XP_011523697.1:p.Phe386=
XM_011525396.2:c.1158C>T (DGKE)	XP_011523698.1:p.Phe386=
XM_017025243.2:c.1476C>T (DGKE)	XP_016880732.1:p.Phe492=
XM_017025244.2:c.1158C>T (DGKE)	XP_016880733.1:p.Phe386=
XR_001752670.2:n.1662C>T (DGKE)
XR_001752671.1:n.1269C>T (DGKE)
XR_001752672.1:n.1270C>T (DGKE)
XR_002958079.1:n.1268C>T (DGKE)
NM_003647.3:c.1104C>T (DGKE) MANE Select	NP_003638.1:p.Phe368=