Canonical Allele Identifier: CA2503156471

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56843968_56843970del , CM000679.2:g.56843968_56843970del GRCh38
NC_000017.10:g.54921329_54921331del , CM000679.1:g.54921329_54921331del GRCh37
NC_000017.9:g.52276328_52276330del NCBI36
NG_033888.1:g.14870_14872del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.465-51_465-49del (DGKE) MANE Select ENSP00000284061.3:n.465-51_465-49del
ENST00000648772.1:c.*314-180_*314-178del (TRIM25) ENSP00000498158.1:n.*314-180_*314-178del
ENST00000284061.7:c.465-51_465-49del (DGKE) ENSP00000284061.3:n.465-51_465-49del
ENST00000572944.1:c.295-51_295-49del (DGKE)
ENST00000576869.5:n.613-51_613-49del (DGKE)
NM_003647.2:c.465-51_465-49del (DGKE) NP_003638.1:n.465-51_465-49del
XM_011525394.1:c.519-51_519-49del (DGKE) XP_011523696.1:n.519-51_519-49del
XM_011525395.1:c.519-51_519-49del (DGKE) XP_011523697.1:n.519-51_519-49del
XM_011525396.1:c.519-51_519-49del (DGKE) XP_011523698.1:n.519-51_519-49del
XM_011525397.1:c.519-51_519-49del (DGKE) XP_011523699.1:n.519-51_519-49del
XM_011525398.1:c.9-51_9-49del (DGKE) XP_011523700.1:n.9-51_9-49del
XR_934581.1:n.618-51_618-49del (DGKE)
XM_011525394.3:c.519-51_519-49del (DGKE) XP_011523696.1:n.519-51_519-49del
XM_011525395.2:c.519-51_519-49del (DGKE) XP_011523697.1:n.519-51_519-49del
XM_011525396.2:c.519-51_519-49del (DGKE) XP_011523698.1:n.519-51_519-49del
XM_017025243.2:c.465-51_465-49del (DGKE) XP_016880732.1:n.465-51_465-49del
XM_017025244.2:c.519-51_519-49del (DGKE) XP_016880733.1:n.519-51_519-49del
XR_001752670.2:n.651-51_651-49del (DGKE)
XR_001752671.1:n.630-51_630-49del (DGKE)
XR_001752672.1:n.631-51_631-49del (DGKE)
XR_002958079.1:n.629-51_629-49del (DGKE)
NM_003647.3:c.465-51_465-49del (DGKE) MANE Select NP_003638.1:n.465-51_465-49del