Canonical Allele Identifier: CA399926957

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845783T>A , CM000679.2:g.56845783T>A GRCh38
NC_000017.10:g.54923144T>A , CM000679.1:g.54923144T>A GRCh37
NC_000017.9:g.52278143T>A NCBI36
NG_033888.1:g.16685T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.718T>A (DGKE) MANE Select ENSP00000284061.3:p.Phe240Ile
ENST00000648772.1:c.*314-1993A>T (TRIM25) ENSP00000498158.1:n.*314-1993A>T
ENST00000284061.7:c.718T>A (DGKE) ENSP00000284061.3:p.Phe240Ile
ENST00000571084.1:n.254T>A (DGKE)
ENST00000572944.1:c.548T>A (DGKE)
ENST00000576869.5:n.866T>A (DGKE)
NM_003647.2:c.718T>A (DGKE) NP_003638.1:p.Phe240Ile
XM_011525394.1:c.772T>A (DGKE) XP_011523696.1:p.Phe258Ile
XM_011525395.1:c.772T>A (DGKE) XP_011523697.1:p.Phe258Ile
XM_011525396.1:c.772T>A (DGKE) XP_011523698.1:p.Phe258Ile
XM_011525397.1:c.772T>A (DGKE) XP_011523699.1:p.Phe258Ile
XM_011525398.1:c.262T>A (DGKE) XP_011523700.1:p.Phe88Ile
XR_934581.1:n.871T>A (DGKE)
XM_011525394.3:c.772T>A (DGKE) XP_011523696.1:p.Phe258Ile
XM_011525395.2:c.772T>A (DGKE) XP_011523697.1:p.Phe258Ile
XM_011525396.2:c.772T>A (DGKE) XP_011523698.1:p.Phe258Ile
XM_017025243.2:c.718T>A (DGKE) XP_016880732.1:p.Phe240Ile
XM_017025244.2:c.772T>A (DGKE) XP_016880733.1:p.Phe258Ile
XR_001752670.2:n.904T>A (DGKE)
XR_001752671.1:n.883T>A (DGKE)
XR_001752672.1:n.884T>A (DGKE)
XR_002958079.1:n.882T>A (DGKE)
NM_003647.3:c.718T>A (DGKE) MANE Select NP_003638.1:p.Phe240Ile