Canonical Allele Identifier: CA2595898819

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848930_56848931insCTC , CM000679.2:g.56848930_56848931insCTC GRCh38
NC_000017.10:g.54926291_54926292insCTC , CM000679.1:g.54926291_54926292insCTC GRCh37
NC_000017.9:g.52281290_52281291insCTC NCBI36
NG_033888.1:g.19832_19833insCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1046+77_1046+78insCTC (DGKE) MANE Select ENSP00000284061.3:n.1046+77_1046+78insCTC
ENST00000648772.1:c.*313+3012_*313+3013insGAG (TRIM25) ENSP00000498158.1:n.*313+3012_*313+3013insGAG
ENST00000284061.7:c.1046+77_1046+78insCTC (DGKE) ENSP00000284061.3:n.1046+77_1046+78insCTC
ENST00000572944.1:c.876+77_876+78insCTC (DGKE)
NM_003647.2:c.1046+77_1046+78insCTC (DGKE) NP_003638.1:n.1046+77_1046+78insCTC
XM_011525394.1:c.1100+77_1100+78insCTC (DGKE) XP_011523696.1:n.1100+77_1100+78insCTC
XM_011525395.1:c.1100+77_1100+78insCTC (DGKE) XP_011523697.1:n.1100+77_1100+78insCTC
XM_011525396.1:c.1100+77_1100+78insCTC (DGKE) XP_011523698.1:n.1100+77_1100+78insCTC
XM_011525397.1:c.1100+77_1100+78insCTC (DGKE) XP_011523699.1:n.1100+77_1100+78insCTC
XM_011525398.1:c.590+77_590+78insCTC (DGKE) XP_011523700.1:n.590+77_590+78insCTC
XR_934581.1:n.1199+77_1199+78insCTC (DGKE)
XM_011525394.3:c.1100+77_1100+78insCTC (DGKE) XP_011523696.1:n.1100+77_1100+78insCTC
XM_011525395.2:c.1100+77_1100+78insCTC (DGKE) XP_011523697.1:n.1100+77_1100+78insCTC
XM_011525396.2:c.1100+77_1100+78insCTC (DGKE) XP_011523698.1:n.1100+77_1100+78insCTC
XM_017025243.2:c.1418+77_1418+78insCTC (DGKE) XP_016880732.1:n.1418+77_1418+78insCTC
XM_017025244.2:c.1100+77_1100+78insCTC (DGKE) XP_016880733.1:n.1100+77_1100+78insCTC
XR_001752670.2:n.1604+77_1604+78insCTC (DGKE)
XR_001752671.1:n.1211+77_1211+78insCTC (DGKE)
XR_001752672.1:n.1212+77_1212+78insCTC (DGKE)
XR_002958079.1:n.1210+77_1210+78insCTC (DGKE)
NM_003647.3:c.1046+77_1046+78insCTC (DGKE) MANE Select NP_003638.1:n.1046+77_1046+78insCTC