Canonical Allele Identifier: CA500665013

Gene: TRIM25 DGKE

Linked Data

• MyVariant Identifiers: chr17:g.54933983T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56856622T>C , CM000679.2:g.56856622T>C	GRCh38
NC_000017.10:g.54933983T>C , CM000679.1:g.54933983T>C	GRCh37
NC_000017.9:g.52288982T>C	NCBI36
NG_033888.1:g.27524T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682766.1:c.1364-1512A>G (TRIM25)	ENSP00000507876.1:n.1364-1512A>G
ENST00000284061.8:c.1209T>C (DGKE) MANE Select	ENSP00000284061.3:p.Asn403=
ENST00000648772.1:c.1364-1512A>G (TRIM25)	ENSP00000498158.1:n.1364-1512A>G
ENST00000284061.7:c.1209T>C (DGKE)	ENSP00000284061.3:p.Asn403=
ENST00000572944.1:c.1039T>C (DGKE)
NM_003647.2:c.1209T>C (DGKE)	NP_003638.1:p.Asn403=
XM_011525394.1:c.1263T>C (DGKE)	XP_011523696.1:p.Asn421=
XM_011525395.1:c.1263T>C (DGKE)	XP_011523697.1:p.Asn421=
XM_011525396.1:c.1263T>C (DGKE)	XP_011523698.1:p.Asn421=
XM_011525397.1:c.1263T>C (DGKE)	XP_011523699.1:p.Asn421=
XM_011525398.1:c.753T>C (DGKE)	XP_011523700.1:p.Asn251=
XR_934581.1:n.1362T>C (DGKE)
XM_011525394.3:c.1263T>C (DGKE)	XP_011523696.1:p.Asn421=
XM_011525395.2:c.1263T>C (DGKE)	XP_011523697.1:p.Asn421=
XM_011525396.2:c.1263T>C (DGKE)	XP_011523698.1:p.Asn421=
XM_017025243.2:c.1581T>C (DGKE)	XP_016880732.1:p.Asn527=
XM_017025244.2:c.1263T>C (DGKE)	XP_016880733.1:p.Asn421=
XR_001752670.2:n.1767T>C (DGKE)
XR_001752671.1:n.1374T>C (DGKE)
XR_001752672.1:n.1375T>C (DGKE)
XR_002958079.1:n.1373T>C (DGKE)
NM_003647.3:c.1209T>C (DGKE) MANE Select	NP_003638.1:p.Asn403=