Canonical Allele Identifier: CA984903511

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848945_56848946insTC , CM000679.2:g.56848945_56848946insTC GRCh38
NC_000017.10:g.54926306_54926307insTC , CM000679.1:g.54926306_54926307insTC GRCh37
NC_000017.9:g.52281305_52281306insTC NCBI36
NG_033888.1:g.19847_19848insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+92_1046+93insTC (DGKE) MANE Select ENSP00000284061.3:n.1046+92_1046+93insTC
ENST00000648772.1:c.*313+2997_*313+2998insGA (TRIM25) ENSP00000498158.1:n.*313+2997_*313+2998insGA
ENST00000284061.7:c.1046+92_1046+93insTC (DGKE) ENSP00000284061.3:n.1046+92_1046+93insTC
ENST00000572944.1:c.876+92_876+93insTC (DGKE)
NM_003647.2:c.1046+92_1046+93insTC (DGKE) NP_003638.1:n.1046+92_1046+93insTC
XM_011525394.1:c.1100+92_1100+93insTC (DGKE) XP_011523696.1:n.1100+92_1100+93insTC
XM_011525395.1:c.1100+92_1100+93insTC (DGKE) XP_011523697.1:n.1100+92_1100+93insTC
XM_011525396.1:c.1100+92_1100+93insTC (DGKE) XP_011523698.1:n.1100+92_1100+93insTC
XM_011525397.1:c.1100+92_1100+93insTC (DGKE) XP_011523699.1:n.1100+92_1100+93insTC
XM_011525398.1:c.590+92_590+93insTC (DGKE) XP_011523700.1:n.590+92_590+93insTC
XR_934581.1:n.1199+92_1199+93insTC (DGKE)
XM_011525394.3:c.1100+92_1100+93insTC (DGKE) XP_011523696.1:n.1100+92_1100+93insTC
XM_011525395.2:c.1100+92_1100+93insTC (DGKE) XP_011523697.1:n.1100+92_1100+93insTC
XM_011525396.2:c.1100+92_1100+93insTC (DGKE) XP_011523698.1:n.1100+92_1100+93insTC
XM_017025243.2:c.1418+92_1418+93insTC (DGKE) XP_016880732.1:n.1418+92_1418+93insTC
XM_017025244.2:c.1100+92_1100+93insTC (DGKE) XP_016880733.1:n.1100+92_1100+93insTC
XR_001752670.2:n.1604+92_1604+93insTC (DGKE)
XR_001752671.1:n.1211+92_1211+93insTC (DGKE)
XR_001752672.1:n.1212+92_1212+93insTC (DGKE)
XR_002958079.1:n.1210+92_1210+93insTC (DGKE)
NM_003647.3:c.1046+92_1046+93insTC (DGKE) MANE Select NP_003638.1:n.1046+92_1046+93insTC