Canonical Allele Identifier: CA773368031

Linked Data

dbSNP Id: rs1318177335

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56846029_56846034del , CM000679.2:g.56846029_56846034del GRCh38
NC_000017.10:g.54923390_54923395del , CM000679.1:g.54923390_54923395del GRCh37
NC_000017.9:g.52278389_52278394del NCBI36
NG_033888.1:g.16931_16936del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.744+220_744+225del (DGKE) MANE Select ENSP00000284061.3:n.744+220_744+225del
ENST00000648772.1:c.*314-2238_*314-2233del (TRIM25) ENSP00000498158.1:n.*314-2238_*314-2233del
ENST00000284061.7:c.744+220_744+225del (DGKE) ENSP00000284061.3:n.744+220_744+225del
ENST00000571084.1:n.500_505del (DGKE)
ENST00000572944.1:c.574+220_574+225del (DGKE)
ENST00000576869.5:n.892+220_892+225del (DGKE)
NM_003647.2:c.744+220_744+225del (DGKE) NP_003638.1:n.744+220_744+225del
XM_011525394.1:c.798+220_798+225del (DGKE) XP_011523696.1:n.798+220_798+225del
XM_011525395.1:c.798+220_798+225del (DGKE) XP_011523697.1:n.798+220_798+225del
XM_011525396.1:c.798+220_798+225del (DGKE) XP_011523698.1:n.798+220_798+225del
XM_011525397.1:c.798+220_798+225del (DGKE) XP_011523699.1:n.798+220_798+225del
XM_011525398.1:c.288+220_288+225del (DGKE) XP_011523700.1:n.288+220_288+225del
XR_934581.1:n.897+220_897+225del (DGKE)
XM_011525394.3:c.798+220_798+225del (DGKE) XP_011523696.1:n.798+220_798+225del
XM_011525395.2:c.798+220_798+225del (DGKE) XP_011523697.1:n.798+220_798+225del
XM_011525396.2:c.798+220_798+225del (DGKE) XP_011523698.1:n.798+220_798+225del
XM_017025243.2:c.744+220_744+225del (DGKE) XP_016880732.1:n.744+220_744+225del
XM_017025244.2:c.798+220_798+225del (DGKE) XP_016880733.1:n.798+220_798+225del
XR_001752670.2:n.930+220_930+225del (DGKE)
XR_001752671.1:n.909+220_909+225del (DGKE)
XR_001752672.1:n.910+220_910+225del (DGKE)
XR_002958079.1:n.908+220_908+225del (DGKE)
NM_003647.3:c.744+220_744+225del (DGKE) MANE Select NP_003638.1:n.744+220_744+225del