Canonical Allele Identifier: CA399905626

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56856564T>A , CM000679.2:g.56856564T>A GRCh38
NC_000017.10:g.54933925T>A , CM000679.1:g.54933925T>A GRCh37
NC_000017.9:g.52288924T>A NCBI36
NG_033888.1:g.27466T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682766.1:c.1364-1454A>T (TRIM25) ENSP00000507876.1:n.1364-1454A>T
ENST00000284061.8:c.1151T>A (DGKE) MANE Select ENSP00000284061.3:p.Leu384His
ENST00000648772.1:c.1364-1454A>T (TRIM25) ENSP00000498158.1:n.1364-1454A>T
ENST00000284061.7:c.1151T>A (DGKE) ENSP00000284061.3:p.Leu384His
ENST00000572944.1:c.981T>A (DGKE)
NM_003647.2:c.1151T>A (DGKE) NP_003638.1:p.Leu384His
XM_011525394.1:c.1205T>A (DGKE) XP_011523696.1:p.Leu402His
XM_011525395.1:c.1205T>A (DGKE) XP_011523697.1:p.Leu402His
XM_011525396.1:c.1205T>A (DGKE) XP_011523698.1:p.Leu402His
XM_011525397.1:c.1205T>A (DGKE) XP_011523699.1:p.Leu402His
XM_011525398.1:c.695T>A (DGKE) XP_011523700.1:p.Leu232His
XR_934581.1:n.1304T>A (DGKE)
XM_011525394.3:c.1205T>A (DGKE) XP_011523696.1:p.Leu402His
XM_011525395.2:c.1205T>A (DGKE) XP_011523697.1:p.Leu402His
XM_011525396.2:c.1205T>A (DGKE) XP_011523698.1:p.Leu402His
XM_017025243.2:c.1523T>A (DGKE) XP_016880732.1:p.Leu508His
XM_017025244.2:c.1205T>A (DGKE) XP_016880733.1:p.Leu402His
XR_001752670.2:n.1709T>A (DGKE)
XR_001752671.1:n.1316T>A (DGKE)
XR_001752672.1:n.1317T>A (DGKE)
XR_002958079.1:n.1315T>A (DGKE)
NM_003647.3:c.1151T>A (DGKE) MANE Select NP_003638.1:p.Leu384His