Canonical Allele Identifier: CA500687333

Gene: DGKE TRIM25

Linked Data

• dbSNP Id: rs1907465363
• MyVariant Identifiers: chr17:g.54926131T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56848770T>G , CM000679.2:g.56848770T>G	GRCh38
NC_000017.10:g.54926131T>G , CM000679.1:g.54926131T>G	GRCh37
NC_000017.9:g.52281130T>G	NCBI36
NG_033888.1:g.19672T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284061.8:c.963T>G (DGKE) MANE Select	ENSP00000284061.3:p.Gly321=
ENST00000648772.1:c.*313+3173A>C (TRIM25)	ENSP00000498158.1:n.*313+3173A>C
ENST00000284061.7:c.963T>G (DGKE)	ENSP00000284061.3:p.Gly321=
ENST00000572944.1:c.793T>G (DGKE)
NM_003647.2:c.963T>G (DGKE)	NP_003638.1:p.Gly321=
XM_011525394.1:c.1017T>G (DGKE)	XP_011523696.1:p.Gly339=
XM_011525395.1:c.1017T>G (DGKE)	XP_011523697.1:p.Gly339=
XM_011525396.1:c.1017T>G (DGKE)	XP_011523698.1:p.Gly339=
XM_011525397.1:c.1017T>G (DGKE)	XP_011523699.1:p.Gly339=
XM_011525398.1:c.507T>G (DGKE)	XP_011523700.1:p.Gly169=
XR_934581.1:n.1116T>G (DGKE)
XM_011525394.3:c.1017T>G (DGKE)	XP_011523696.1:p.Gly339=
XM_011525395.2:c.1017T>G (DGKE)	XP_011523697.1:p.Gly339=
XM_011525396.2:c.1017T>G (DGKE)	XP_011523698.1:p.Gly339=
XM_017025243.2:c.1335T>G (DGKE)	XP_016880732.1:p.Gly445=
XM_017025244.2:c.1017T>G (DGKE)	XP_016880733.1:p.Gly339=
XR_001752670.2:n.1521T>G (DGKE)
XR_001752671.1:n.1128T>G (DGKE)
XR_001752672.1:n.1129T>G (DGKE)
XR_002958079.1:n.1127T>G (DGKE)
NM_003647.3:c.963T>G (DGKE) MANE Select	NP_003638.1:p.Gly321=