Canonical Allele Identifier: CA2638886941

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848921_56848922dup , CM000679.2:g.56848921_56848922dup GRCh38
NC_000017.10:g.54926282_54926283dup , CM000679.1:g.54926282_54926283dup GRCh37
NC_000017.9:g.52281281_52281282dup NCBI36
NG_033888.1:g.19823_19824dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+68_1046+69dup (DGKE) MANE Select ENSP00000284061.3:n.1046+68_1046+69dup
ENST00000648772.1:c.*313+3021_*313+3022dup (TRIM25) ENSP00000498158.1:n.*313+3021_*313+3022dup
ENST00000284061.7:c.1046+68_1046+69dup (DGKE) ENSP00000284061.3:n.1046+68_1046+69dup
ENST00000572944.1:c.876+68_876+69dup (DGKE)
NM_003647.2:c.1046+68_1046+69dup (DGKE) NP_003638.1:n.1046+68_1046+69dup
XM_011525394.1:c.1100+68_1100+69dup (DGKE) XP_011523696.1:n.1100+68_1100+69dup
XM_011525395.1:c.1100+68_1100+69dup (DGKE) XP_011523697.1:n.1100+68_1100+69dup
XM_011525396.1:c.1100+68_1100+69dup (DGKE) XP_011523698.1:n.1100+68_1100+69dup
XM_011525397.1:c.1100+68_1100+69dup (DGKE) XP_011523699.1:n.1100+68_1100+69dup
XM_011525398.1:c.590+68_590+69dup (DGKE) XP_011523700.1:n.590+68_590+69dup
XR_934581.1:n.1199+68_1199+69dup (DGKE)
XM_011525394.3:c.1100+68_1100+69dup (DGKE) XP_011523696.1:n.1100+68_1100+69dup
XM_011525395.2:c.1100+68_1100+69dup (DGKE) XP_011523697.1:n.1100+68_1100+69dup
XM_011525396.2:c.1100+68_1100+69dup (DGKE) XP_011523698.1:n.1100+68_1100+69dup
XM_017025243.2:c.1418+68_1418+69dup (DGKE) XP_016880732.1:n.1418+68_1418+69dup
XM_017025244.2:c.1100+68_1100+69dup (DGKE) XP_016880733.1:n.1100+68_1100+69dup
XR_001752670.2:n.1604+68_1604+69dup (DGKE)
XR_001752671.1:n.1211+68_1211+69dup (DGKE)
XR_001752672.1:n.1212+68_1212+69dup (DGKE)
XR_002958079.1:n.1210+68_1210+69dup (DGKE)
NM_003647.3:c.1046+68_1046+69dup (DGKE) MANE Select NP_003638.1:n.1046+68_1046+69dup