Canonical Allele Identifier: CA2638885820

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845893_56845894dup , CM000679.2:g.56845893_56845894dup GRCh38
NC_000017.10:g.54923254_54923255dup , CM000679.1:g.54923254_54923255dup GRCh37
NC_000017.9:g.52278253_52278254dup NCBI36
NG_033888.1:g.16795_16796dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.744+84_744+85dup (DGKE) MANE Select ENSP00000284061.3:n.744+84_744+85dup
ENST00000648772.1:c.*314-2103_*314-2102dup (TRIM25) ENSP00000498158.1:n.*314-2103_*314-2102dup
ENST00000284061.7:c.744+84_744+85dup (DGKE) ENSP00000284061.3:n.744+84_744+85dup
ENST00000571084.1:n.364_365dup (DGKE)
ENST00000572944.1:c.574+84_574+85dup (DGKE)
ENST00000576869.5:n.892+84_892+85dup (DGKE)
NM_003647.2:c.744+84_744+85dup (DGKE) NP_003638.1:n.744+84_744+85dup
XM_011525394.1:c.798+84_798+85dup (DGKE) XP_011523696.1:n.798+84_798+85dup
XM_011525395.1:c.798+84_798+85dup (DGKE) XP_011523697.1:n.798+84_798+85dup
XM_011525396.1:c.798+84_798+85dup (DGKE) XP_011523698.1:n.798+84_798+85dup
XM_011525397.1:c.798+84_798+85dup (DGKE) XP_011523699.1:n.798+84_798+85dup
XM_011525398.1:c.288+84_288+85dup (DGKE) XP_011523700.1:n.288+84_288+85dup
XR_934581.1:n.897+84_897+85dup (DGKE)
XM_011525394.3:c.798+84_798+85dup (DGKE) XP_011523696.1:n.798+84_798+85dup
XM_011525395.2:c.798+84_798+85dup (DGKE) XP_011523697.1:n.798+84_798+85dup
XM_011525396.2:c.798+84_798+85dup (DGKE) XP_011523698.1:n.798+84_798+85dup
XM_017025243.2:c.744+84_744+85dup (DGKE) XP_016880732.1:n.744+84_744+85dup
XM_017025244.2:c.798+84_798+85dup (DGKE) XP_016880733.1:n.798+84_798+85dup
XR_001752670.2:n.930+84_930+85dup (DGKE)
XR_001752671.1:n.909+84_909+85dup (DGKE)
XR_001752672.1:n.910+84_910+85dup (DGKE)
XR_002958079.1:n.908+84_908+85dup (DGKE)
NM_003647.3:c.744+84_744+85dup (DGKE) MANE Select NP_003638.1:n.744+84_744+85dup