Canonical Allele Identifier: CA2266993663

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845705G= , CM000679.2:g.56845705G= GRCh38
NC_000017.10:g.54923066G= , CM000679.1:g.54923066G= GRCh37
NC_000017.9:g.52278065G= NCBI36
NG_033888.1:g.16607G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.640G= (DGKE) MANE Select ENSP00000284061.3:p.Gly214=
ENST00000648772.1:c.*314-1915C= (TRIM25) ENSP00000498158.1:n.*314-1915C=
ENST00000284061.7:c.640G= (DGKE) ENSP00000284061.3:p.Gly214=
ENST00000571084.1:n.176G= (DGKE)
ENST00000572944.1:c.470G= (DGKE)
ENST00000576869.5:n.788G= (DGKE)
NM_003647.2:c.640G= (DGKE) NP_003638.1:p.Gly214=
XM_011525394.1:c.694G= (DGKE) XP_011523696.1:p.Gly232=
XM_011525395.1:c.694G= (DGKE) XP_011523697.1:p.Gly232=
XM_011525396.1:c.694G= (DGKE) XP_011523698.1:p.Gly232=
XM_011525397.1:c.694G= (DGKE) XP_011523699.1:p.Gly232=
XM_011525398.1:c.184G= (DGKE) XP_011523700.1:p.Gly62=
XR_934581.1:n.793G= (DGKE)
XM_011525394.3:c.694G= (DGKE) XP_011523696.1:p.Gly232=
XM_011525395.2:c.694G= (DGKE) XP_011523697.1:p.Gly232=
XM_011525396.2:c.694G= (DGKE) XP_011523698.1:p.Gly232=
XM_017025243.2:c.640G= (DGKE) XP_016880732.1:p.Gly214=
XM_017025244.2:c.694G= (DGKE) XP_016880733.1:p.Gly232=
XR_001752670.2:n.826G= (DGKE)
XR_001752671.1:n.805G= (DGKE)
XR_001752672.1:n.806G= (DGKE)
XR_002958079.1:n.804G= (DGKE)
NM_003647.3:c.640G= (DGKE) MANE Select NP_003638.1:p.Gly214=