Canonical Allele Identifier: CA399905600

Gene: TRIM25 DGKE

Linked Data

• MyVariant Identifiers: chr17:g.54933912G>T (hg19) ; chr17:g.56856551G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56856551G>T , CM000679.2:g.56856551G>T	GRCh38
NC_000017.10:g.54933912G>T , CM000679.1:g.54933912G>T	GRCh37
NC_000017.9:g.52288911G>T	NCBI36
NG_033888.1:g.27453G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682766.1:c.1364-1441C>A (TRIM25)	ENSP00000507876.1:n.1364-1441C>A
ENST00000284061.8:c.1138G>T (DGKE) MANE Select	ENSP00000284061.3:p.Ala380Ser
ENST00000648772.1:c.1364-1441C>A (TRIM25)	ENSP00000498158.1:n.1364-1441C>A
ENST00000284061.7:c.1138G>T (DGKE)	ENSP00000284061.3:p.Ala380Ser
ENST00000572944.1:c.968G>T (DGKE)
NM_003647.2:c.1138G>T (DGKE)	NP_003638.1:p.Ala380Ser
XM_011525394.1:c.1192G>T (DGKE)	XP_011523696.1:p.Ala398Ser
XM_011525395.1:c.1192G>T (DGKE)	XP_011523697.1:p.Ala398Ser
XM_011525396.1:c.1192G>T (DGKE)	XP_011523698.1:p.Ala398Ser
XM_011525397.1:c.1192G>T (DGKE)	XP_011523699.1:p.Ala398Ser
XM_011525398.1:c.682G>T (DGKE)	XP_011523700.1:p.Ala228Ser
XR_934581.1:n.1291G>T (DGKE)
XM_011525394.3:c.1192G>T (DGKE)	XP_011523696.1:p.Ala398Ser
XM_011525395.2:c.1192G>T (DGKE)	XP_011523697.1:p.Ala398Ser
XM_011525396.2:c.1192G>T (DGKE)	XP_011523698.1:p.Ala398Ser
XM_017025243.2:c.1510G>T (DGKE)	XP_016880732.1:p.Ala504Ser
XM_017025244.2:c.1192G>T (DGKE)	XP_016880733.1:p.Ala398Ser
XR_001752670.2:n.1696G>T (DGKE)
XR_001752671.1:n.1303G>T (DGKE)
XR_001752672.1:n.1304G>T (DGKE)
XR_002958079.1:n.1302G>T (DGKE)
NM_003647.3:c.1138G>T (DGKE) MANE Select	NP_003638.1:p.Ala380Ser