Canonical Allele Identifier: CA2266998713

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56856619T= , CM000679.2:g.56856619T= GRCh38
NC_000017.10:g.54933980T= , CM000679.1:g.54933980T= GRCh37
NC_000017.9:g.52288979T= NCBI36
NG_033888.1:g.27521T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682766.1:c.1364-1509A= (TRIM25) ENSP00000507876.1:n.1364-1509A=
ENST00000284061.8:c.1206T= (DGKE) MANE Select ENSP00000284061.3:p.Leu402=
ENST00000648772.1:c.1364-1509A= (TRIM25) ENSP00000498158.1:n.1364-1509A=
ENST00000284061.7:c.1206T= (DGKE) ENSP00000284061.3:p.Leu402=
ENST00000572944.1:c.1036T= (DGKE)
NM_003647.2:c.1206T= (DGKE) NP_003638.1:p.Leu402=
XM_011525394.1:c.1260T= (DGKE) XP_011523696.1:p.Leu420=
XM_011525395.1:c.1260T= (DGKE) XP_011523697.1:p.Leu420=
XM_011525396.1:c.1260T= (DGKE) XP_011523698.1:p.Leu420=
XM_011525397.1:c.1260T= (DGKE) XP_011523699.1:p.Leu420=
XM_011525398.1:c.750T= (DGKE) XP_011523700.1:p.Leu250=
XR_934581.1:n.1359T= (DGKE)
XM_011525394.3:c.1260T= (DGKE) XP_011523696.1:p.Leu420=
XM_011525395.2:c.1260T= (DGKE) XP_011523697.1:p.Leu420=
XM_011525396.2:c.1260T= (DGKE) XP_011523698.1:p.Leu420=
XM_017025243.2:c.1578T= (DGKE) XP_016880732.1:p.Leu526=
XM_017025244.2:c.1260T= (DGKE) XP_016880733.1:p.Leu420=
XR_001752670.2:n.1764T= (DGKE)
XR_001752671.1:n.1371T= (DGKE)
XR_001752672.1:n.1372T= (DGKE)
XR_002958079.1:n.1370T= (DGKE)
NM_003647.3:c.1206T= (DGKE) MANE Select NP_003638.1:p.Leu402=