Canonical Allele Identifier: CA2501972016

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845548_56845549insAGAC , CM000679.2:g.56845548_56845549insAGAC GRCh38
NC_000017.10:g.54922909_54922910insAGAC , CM000679.1:g.54922909_54922910insAGAC GRCh37
NC_000017.9:g.52277908_52277909insAGAC NCBI36
NG_033888.1:g.16450_16451insAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.625-142_625-141insAGAC (DGKE) MANE Select ENSP00000284061.3:n.625-142_625-141insAGAC
ENST00000648772.1:c.*314-1759_*314-1758insGTCT (TRIM25) ENSP00000498158.1:n.*314-1759_*314-1758insGTCT
ENST00000284061.7:c.625-142_625-141insAGAC (DGKE) ENSP00000284061.3:n.625-142_625-141insAGAC
ENST00000571084.1:n.161-142_161-141insAGAC (DGKE)
ENST00000572944.1:c.455-142_455-141insAGAC (DGKE)
ENST00000576869.5:n.773-142_773-141insAGAC (DGKE)
NM_003647.2:c.625-142_625-141insAGAC (DGKE) NP_003638.1:n.625-142_625-141insAGAC
XM_011525394.1:c.679-142_679-141insAGAC (DGKE) XP_011523696.1:n.679-142_679-141insAGAC
XM_011525395.1:c.679-142_679-141insAGAC (DGKE) XP_011523697.1:n.679-142_679-141insAGAC
XM_011525396.1:c.679-142_679-141insAGAC (DGKE) XP_011523698.1:n.679-142_679-141insAGAC
XM_011525397.1:c.679-142_679-141insAGAC (DGKE) XP_011523699.1:n.679-142_679-141insAGAC
XM_011525398.1:c.169-142_169-141insAGAC (DGKE) XP_011523700.1:n.169-142_169-141insAGAC
XR_934581.1:n.778-142_778-141insAGAC (DGKE)
XM_011525394.3:c.679-142_679-141insAGAC (DGKE) XP_011523696.1:n.679-142_679-141insAGAC
XM_011525395.2:c.679-142_679-141insAGAC (DGKE) XP_011523697.1:n.679-142_679-141insAGAC
XM_011525396.2:c.679-142_679-141insAGAC (DGKE) XP_011523698.1:n.679-142_679-141insAGAC
XM_017025243.2:c.625-142_625-141insAGAC (DGKE) XP_016880732.1:n.625-142_625-141insAGAC
XM_017025244.2:c.679-142_679-141insAGAC (DGKE) XP_016880733.1:n.679-142_679-141insAGAC
XR_001752670.2:n.811-142_811-141insAGAC (DGKE)
XR_001752671.1:n.790-142_790-141insAGAC (DGKE)
XR_001752672.1:n.791-142_791-141insAGAC (DGKE)
XR_002958079.1:n.789-142_789-141insAGAC (DGKE)
NM_003647.3:c.625-142_625-141insAGAC (DGKE) MANE Select NP_003638.1:n.625-142_625-141insAGAC