Canonical Allele Identifier: CA291907935
Community Standard Title: NM_003647.3(DGKE):c.888+69_888+70dup

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848134_56848135dup , CM000679.2:g.56848134_56848135dup GRCh38
NC_000017.10:g.54925495_54925496dup , CM000679.1:g.54925495_54925496dup GRCh37
NC_000017.9:g.52280494_52280495dup NCBI36
NG_033888.1:g.19036_19037dup

Transcript Alleles

HGVS Amino-acid Change
NM_003647.3:c.888+69_888+70dup (DGKE) MANE Select NP_003638.1:n.888+69_888+70dup
ENST00000284061.8:c.888+69_888+70dup (DGKE) MANE Select ENSP00000284061.3:n.888+69_888+70dup
NM_003647.2:c.888+69_888+70dup (DGKE) NP_003638.1:n.888+69_888+70dup
ENST00000284061.7:c.888+69_888+70dup (DGKE) ENSP00000284061.3:n.888+69_888+70dup
ENST00000572944.1:c.718+69_718+70dup (DGKE)
ENST00000648772.1:c.*313+3822_*313+3823dup (TRIM25) ENSP00000498158.1:n.*313+3822_*313+3823dup
XM_011525394.1:c.942+69_942+70dup (DGKE) XP_011523696.1:n.942+69_942+70dup
XM_011525394.3:c.942+69_942+70dup (DGKE) XP_011523696.1:n.942+69_942+70dup
XM_011525395.1:c.942+69_942+70dup (DGKE) XP_011523697.1:n.942+69_942+70dup
XM_011525395.2:c.942+69_942+70dup (DGKE) XP_011523697.1:n.942+69_942+70dup
XM_011525396.1:c.942+69_942+70dup (DGKE) XP_011523698.1:n.942+69_942+70dup
XM_011525396.2:c.942+69_942+70dup (DGKE) XP_011523698.1:n.942+69_942+70dup
XM_011525397.1:c.942+69_942+70dup (DGKE) XP_011523699.1:n.942+69_942+70dup
XM_011525398.1:c.432+69_432+70dup (DGKE) XP_011523700.1:n.432+69_432+70dup
XM_017025243.2:c.957_958dup (DGKE) XP_016880732.1:p.Trp320TyrfsTer15
XM_017025244.2:c.942+69_942+70dup (DGKE) XP_016880733.1:n.942+69_942+70dup
XR_001752670.2:n.1143_1144dup (DGKE)
XR_001752671.1:n.1053+69_1053+70dup (DGKE)
XR_001752672.1:n.1054+69_1054+70dup (DGKE)
XR_002958079.1:n.1052+69_1052+70dup (DGKE)
XR_934581.1:n.1041+69_1041+70dup (DGKE)