Canonical Allele Identifier: CA399905638

Gene: TRIM25 DGKE

Linked Data

• MyVariant Identifiers: chr17:g.54933930T>G (hg19) ; chr17:g.56856569T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56856569T>G , CM000679.2:g.56856569T>G	GRCh38
NC_000017.10:g.54933930T>G , CM000679.1:g.54933930T>G	GRCh37
NC_000017.9:g.52288929T>G	NCBI36
NG_033888.1:g.27471T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682766.1:c.1364-1459A>C (TRIM25)	ENSP00000507876.1:n.1364-1459A>C
ENST00000284061.8:c.1156T>G (DGKE) MANE Select	ENSP00000284061.3:p.Phe386Val
ENST00000648772.1:c.1364-1459A>C (TRIM25)	ENSP00000498158.1:n.1364-1459A>C
ENST00000284061.7:c.1156T>G (DGKE)	ENSP00000284061.3:p.Phe386Val
ENST00000572944.1:c.986T>G (DGKE)
NM_003647.2:c.1156T>G (DGKE)	NP_003638.1:p.Phe386Val
XM_011525394.1:c.1210T>G (DGKE)	XP_011523696.1:p.Phe404Val
XM_011525395.1:c.1210T>G (DGKE)	XP_011523697.1:p.Phe404Val
XM_011525396.1:c.1210T>G (DGKE)	XP_011523698.1:p.Phe404Val
XM_011525397.1:c.1210T>G (DGKE)	XP_011523699.1:p.Phe404Val
XM_011525398.1:c.700T>G (DGKE)	XP_011523700.1:p.Phe234Val
XR_934581.1:n.1309T>G (DGKE)
XM_011525394.3:c.1210T>G (DGKE)	XP_011523696.1:p.Phe404Val
XM_011525395.2:c.1210T>G (DGKE)	XP_011523697.1:p.Phe404Val
XM_011525396.2:c.1210T>G (DGKE)	XP_011523698.1:p.Phe404Val
XM_017025243.2:c.1528T>G (DGKE)	XP_016880732.1:p.Phe510Val
XM_017025244.2:c.1210T>G (DGKE)	XP_016880733.1:p.Phe404Val
XR_001752670.2:n.1714T>G (DGKE)
XR_001752671.1:n.1321T>G (DGKE)
XR_001752672.1:n.1322T>G (DGKE)
XR_002958079.1:n.1320T>G (DGKE)
NM_003647.3:c.1156T>G (DGKE) MANE Select	NP_003638.1:p.Phe386Val