Canonical Allele Identifier: CA2266993709

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845819_56845823delinsGAAAA , CM000679.2:g.56845819_56845823delinsGAAAA GRCh38
NC_000017.10:g.54923180_54923184delinsGAAAA , CM000679.1:g.54923180_54923184delinsGAAAA GRCh37
NC_000017.9:g.52278179_52278183delinsGAAAA NCBI36
NG_033888.1:g.16721_16725delinsGAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.744+10_744+14delinsGAAAA (DGKE) MANE Select ENSP00000284061.3:n.744+10_744+14delinsGAAAA
ENST00000648772.1:c.*314-2033_*314-2029delinsTTTTC (TRIM25) ENSP00000498158.1:n.*314-2033_*314-2029delinsTTTTC
ENST00000284061.7:c.744+10_744+14delinsGAAAA (DGKE) ENSP00000284061.3:n.744+10_744+14delinsGAAAA
ENST00000571084.1:n.290_294delinsGAAAA (DGKE)
ENST00000572944.1:c.574+10_574+14delinsGAAAA (DGKE)
ENST00000576869.5:n.892+10_892+14delinsGAAAA (DGKE)
NM_003647.2:c.744+10_744+14delinsGAAAA (DGKE) NP_003638.1:n.744+10_744+14delinsGAAAA
XM_011525394.1:c.798+10_798+14delinsGAAAA (DGKE) XP_011523696.1:n.798+10_798+14delinsGAAAA
XM_011525395.1:c.798+10_798+14delinsGAAAA (DGKE) XP_011523697.1:n.798+10_798+14delinsGAAAA
XM_011525396.1:c.798+10_798+14delinsGAAAA (DGKE) XP_011523698.1:n.798+10_798+14delinsGAAAA
XM_011525397.1:c.798+10_798+14delinsGAAAA (DGKE) XP_011523699.1:n.798+10_798+14delinsGAAAA
XM_011525398.1:c.288+10_288+14delinsGAAAA (DGKE) XP_011523700.1:n.288+10_288+14delinsGAAAA
XR_934581.1:n.897+10_897+14delinsGAAAA (DGKE)
XM_011525394.3:c.798+10_798+14delinsGAAAA (DGKE) XP_011523696.1:n.798+10_798+14delinsGAAAA
XM_011525395.2:c.798+10_798+14delinsGAAAA (DGKE) XP_011523697.1:n.798+10_798+14delinsGAAAA
XM_011525396.2:c.798+10_798+14delinsGAAAA (DGKE) XP_011523698.1:n.798+10_798+14delinsGAAAA
XM_017025243.2:c.744+10_744+14delinsGAAAA (DGKE) XP_016880732.1:n.744+10_744+14delinsGAAAA
XM_017025244.2:c.798+10_798+14delinsGAAAA (DGKE) XP_016880733.1:n.798+10_798+14delinsGAAAA
XR_001752670.2:n.930+10_930+14delinsGAAAA (DGKE)
XR_001752671.1:n.909+10_909+14delinsGAAAA (DGKE)
XR_001752672.1:n.910+10_910+14delinsGAAAA (DGKE)
XR_002958079.1:n.908+10_908+14delinsGAAAA (DGKE)
NM_003647.3:c.744+10_744+14delinsGAAAA (DGKE) MANE Select NP_003638.1:n.744+10_744+14delinsGAAAA