Canonical Allele Identifier: CA2638885776

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845826dup , CM000679.2:g.56845826dup GRCh38
NC_000017.10:g.54923187dup , CM000679.1:g.54923187dup GRCh37
NC_000017.9:g.52278186dup NCBI36
NG_033888.1:g.16728dup

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.744+17dup (DGKE) MANE Select ENSP00000284061.3:n.744+17dup
ENST00000648772.1:c.*314-2030dup (TRIM25) ENSP00000498158.1:n.*314-2030dup
ENST00000284061.7:c.744+17dup (DGKE) ENSP00000284061.3:n.744+17dup
ENST00000571084.1:n.297dup (DGKE)
ENST00000572944.1:c.574+17dup (DGKE)
ENST00000576869.5:n.892+17dup (DGKE)
NM_003647.2:c.744+17dup (DGKE) NP_003638.1:n.744+17dup
XM_011525394.1:c.798+17dup (DGKE) XP_011523696.1:n.798+17dup
XM_011525395.1:c.798+17dup (DGKE) XP_011523697.1:n.798+17dup
XM_011525396.1:c.798+17dup (DGKE) XP_011523698.1:n.798+17dup
XM_011525397.1:c.798+17dup (DGKE) XP_011523699.1:n.798+17dup
XM_011525398.1:c.288+17dup (DGKE) XP_011523700.1:n.288+17dup
XR_934581.1:n.897+17dup (DGKE)
XM_011525394.3:c.798+17dup (DGKE) XP_011523696.1:n.798+17dup
XM_011525395.2:c.798+17dup (DGKE) XP_011523697.1:n.798+17dup
XM_011525396.2:c.798+17dup (DGKE) XP_011523698.1:n.798+17dup
XM_017025243.2:c.744+17dup (DGKE) XP_016880732.1:n.744+17dup
XM_017025244.2:c.798+17dup (DGKE) XP_016880733.1:n.798+17dup
XR_001752670.2:n.930+17dup (DGKE)
XR_001752671.1:n.909+17dup (DGKE)
XR_001752672.1:n.910+17dup (DGKE)
XR_002958079.1:n.908+17dup (DGKE)
NM_003647.3:c.744+17dup (DGKE) MANE Select NP_003638.1:n.744+17dup