Canonical Allele Identifier: CA984903503

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848941_56848942del , CM000679.2:g.56848941_56848942del GRCh38
NC_000017.10:g.54926302_54926303del , CM000679.1:g.54926302_54926303del GRCh37
NC_000017.9:g.52281301_52281302del NCBI36
NG_033888.1:g.19843_19844del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+88_1046+89del (DGKE) MANE Select ENSP00000284061.3:n.1046+88_1046+89del
ENST00000648772.1:c.*313+3001_*313+3002del (TRIM25) ENSP00000498158.1:n.*313+3001_*313+3002del
ENST00000284061.7:c.1046+88_1046+89del (DGKE) ENSP00000284061.3:n.1046+88_1046+89del
ENST00000572944.1:c.876+88_876+89del (DGKE)
NM_003647.2:c.1046+88_1046+89del (DGKE) NP_003638.1:n.1046+88_1046+89del
XM_011525394.1:c.1100+88_1100+89del (DGKE) XP_011523696.1:n.1100+88_1100+89del
XM_011525395.1:c.1100+88_1100+89del (DGKE) XP_011523697.1:n.1100+88_1100+89del
XM_011525396.1:c.1100+88_1100+89del (DGKE) XP_011523698.1:n.1100+88_1100+89del
XM_011525397.1:c.1100+88_1100+89del (DGKE) XP_011523699.1:n.1100+88_1100+89del
XM_011525398.1:c.590+88_590+89del (DGKE) XP_011523700.1:n.590+88_590+89del
XR_934581.1:n.1199+88_1199+89del (DGKE)
XM_011525394.3:c.1100+88_1100+89del (DGKE) XP_011523696.1:n.1100+88_1100+89del
XM_011525395.2:c.1100+88_1100+89del (DGKE) XP_011523697.1:n.1100+88_1100+89del
XM_011525396.2:c.1100+88_1100+89del (DGKE) XP_011523698.1:n.1100+88_1100+89del
XM_017025243.2:c.1418+88_1418+89del (DGKE) XP_016880732.1:n.1418+88_1418+89del
XM_017025244.2:c.1100+88_1100+89del (DGKE) XP_016880733.1:n.1100+88_1100+89del
XR_001752670.2:n.1604+88_1604+89del (DGKE)
XR_001752671.1:n.1211+88_1211+89del (DGKE)
XR_001752672.1:n.1212+88_1212+89del (DGKE)
XR_002958079.1:n.1210+88_1210+89del (DGKE)
NM_003647.3:c.1046+88_1046+89del (DGKE) MANE Select NP_003638.1:n.1046+88_1046+89del