Canonical Allele Identifier: CA500664504

Gene: TRIM25 DGKE

Linked Data

• dbSNP Id: rs1907961202
• MyVariant Identifiers: chr17:g.54933908T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56856547T>C , CM000679.2:g.56856547T>C	GRCh38
NC_000017.10:g.54933908T>C , CM000679.1:g.54933908T>C	GRCh37
NC_000017.9:g.52288907T>C	NCBI36
NG_033888.1:g.27449T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682766.1:c.1364-1437A>G (TRIM25)	ENSP00000507876.1:n.1364-1437A>G
ENST00000284061.8:c.1134T>C (DGKE) MANE Select	ENSP00000284061.3:p.Pro378=
ENST00000648772.1:c.1364-1437A>G (TRIM25)	ENSP00000498158.1:n.1364-1437A>G
ENST00000284061.7:c.1134T>C (DGKE)	ENSP00000284061.3:p.Pro378=
ENST00000572944.1:c.964T>C (DGKE)
NM_003647.2:c.1134T>C (DGKE)	NP_003638.1:p.Pro378=
XM_011525394.1:c.1188T>C (DGKE)	XP_011523696.1:p.Pro396=
XM_011525395.1:c.1188T>C (DGKE)	XP_011523697.1:p.Pro396=
XM_011525396.1:c.1188T>C (DGKE)	XP_011523698.1:p.Pro396=
XM_011525397.1:c.1188T>C (DGKE)	XP_011523699.1:p.Pro396=
XM_011525398.1:c.678T>C (DGKE)	XP_011523700.1:p.Pro226=
XR_934581.1:n.1287T>C (DGKE)
XM_011525394.3:c.1188T>C (DGKE)	XP_011523696.1:p.Pro396=
XM_011525395.2:c.1188T>C (DGKE)	XP_011523697.1:p.Pro396=
XM_011525396.2:c.1188T>C (DGKE)	XP_011523698.1:p.Pro396=
XM_017025243.2:c.1506T>C (DGKE)	XP_016880732.1:p.Pro502=
XM_017025244.2:c.1188T>C (DGKE)	XP_016880733.1:p.Pro396=
XR_001752670.2:n.1692T>C (DGKE)
XR_001752671.1:n.1299T>C (DGKE)
XR_001752672.1:n.1300T>C (DGKE)
XR_002958079.1:n.1298T>C (DGKE)
NM_003647.3:c.1134T>C (DGKE) MANE Select	NP_003638.1:p.Pro378=