Canonical Allele Identifier: CA2266995112

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848768G= , CM000679.2:g.56848768G= GRCh38
NC_000017.10:g.54926129G= , CM000679.1:g.54926129G= GRCh37
NC_000017.9:g.52281128G= NCBI36
NG_033888.1:g.19670G=

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.961G= (DGKE) MANE Select ENSP00000284061.3:p.Gly321=
ENST00000648772.1:c.*313+3175C= (TRIM25) ENSP00000498158.1:n.*313+3175C=
ENST00000284061.7:c.961G= (DGKE) ENSP00000284061.3:p.Gly321=
ENST00000572944.1:c.791G= (DGKE)
NM_003647.2:c.961G= (DGKE) NP_003638.1:p.Gly321=
XM_011525394.1:c.1015G= (DGKE) XP_011523696.1:p.Gly339=
XM_011525395.1:c.1015G= (DGKE) XP_011523697.1:p.Gly339=
XM_011525396.1:c.1015G= (DGKE) XP_011523698.1:p.Gly339=
XM_011525397.1:c.1015G= (DGKE) XP_011523699.1:p.Gly339=
XM_011525398.1:c.505G= (DGKE) XP_011523700.1:p.Gly169=
XR_934581.1:n.1114G= (DGKE)
XM_011525394.3:c.1015G= (DGKE) XP_011523696.1:p.Gly339=
XM_011525395.2:c.1015G= (DGKE) XP_011523697.1:p.Gly339=
XM_011525396.2:c.1015G= (DGKE) XP_011523698.1:p.Gly339=
XM_017025243.2:c.1333G= (DGKE) XP_016880732.1:p.Gly445=
XM_017025244.2:c.1015G= (DGKE) XP_016880733.1:p.Gly339=
XR_001752670.2:n.1519G= (DGKE)
XR_001752671.1:n.1126G= (DGKE)
XR_001752672.1:n.1127G= (DGKE)
XR_002958079.1:n.1125G= (DGKE)
NM_003647.3:c.961G= (DGKE) MANE Select NP_003638.1:p.Gly321=