Canonical Allele Identifier: CA2266993804

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56846022_56846028delinsGATAAAT , CM000679.2:g.56846022_56846028delinsGATAAAT GRCh38
NC_000017.10:g.54923383_54923389delinsGATAAAT , CM000679.1:g.54923383_54923389delinsGATAAAT GRCh37
NC_000017.9:g.52278382_52278388delinsGATAAAT NCBI36
NG_033888.1:g.16924_16930delinsGATAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.744+213_744+219delinsGATAAAT (DGKE) MANE Select ENSP00000284061.3:n.744+213_744+219delinsGATAAAT
ENST00000648772.1:c.*314-2238_*314-2232delinsATTTATC (TRIM25) ENSP00000498158.1:n.*314-2238_*314-2232delinsATTTATC
ENST00000284061.7:c.744+213_744+219delinsGATAAAT (DGKE) ENSP00000284061.3:n.744+213_744+219delinsGATAAAT
ENST00000571084.1:n.493_499delinsGATAAAT (DGKE)
ENST00000572944.1:c.574+213_574+219delinsGATAAAT (DGKE)
ENST00000576869.5:n.892+213_892+219delinsGATAAAT (DGKE)
NM_003647.2:c.744+213_744+219delinsGATAAAT (DGKE) NP_003638.1:n.744+213_744+219delinsGATAAAT
XM_011525394.1:c.798+213_798+219delinsGATAAAT (DGKE) XP_011523696.1:n.798+213_798+219delinsGATAAAT
XM_011525395.1:c.798+213_798+219delinsGATAAAT (DGKE) XP_011523697.1:n.798+213_798+219delinsGATAAAT
XM_011525396.1:c.798+213_798+219delinsGATAAAT (DGKE) XP_011523698.1:n.798+213_798+219delinsGATAAAT
XM_011525397.1:c.798+213_798+219delinsGATAAAT (DGKE) XP_011523699.1:n.798+213_798+219delinsGATAAAT
XM_011525398.1:c.288+213_288+219delinsGATAAAT (DGKE) XP_011523700.1:n.288+213_288+219delinsGATAAAT
XR_934581.1:n.897+213_897+219delinsGATAAAT (DGKE)
XM_011525394.3:c.798+213_798+219delinsGATAAAT (DGKE) XP_011523696.1:n.798+213_798+219delinsGATAAAT
XM_011525395.2:c.798+213_798+219delinsGATAAAT (DGKE) XP_011523697.1:n.798+213_798+219delinsGATAAAT
XM_011525396.2:c.798+213_798+219delinsGATAAAT (DGKE) XP_011523698.1:n.798+213_798+219delinsGATAAAT
XM_017025243.2:c.744+213_744+219delinsGATAAAT (DGKE) XP_016880732.1:n.744+213_744+219delinsGATAAAT
XM_017025244.2:c.798+213_798+219delinsGATAAAT (DGKE) XP_016880733.1:n.798+213_798+219delinsGATAAAT
XR_001752670.2:n.930+213_930+219delinsGATAAAT (DGKE)
XR_001752671.1:n.909+213_909+219delinsGATAAAT (DGKE)
XR_001752672.1:n.910+213_910+219delinsGATAAAT (DGKE)
XR_002958079.1:n.908+213_908+219delinsGATAAAT (DGKE)
NM_003647.3:c.744+213_744+219delinsGATAAAT (DGKE) MANE Select NP_003638.1:n.744+213_744+219delinsGATAAAT