Canonical Allele Identifier: CA399927974

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848808A>G , CM000679.2:g.56848808A>G GRCh38
NC_000017.10:g.54926169A>G , CM000679.1:g.54926169A>G GRCh37
NC_000017.9:g.52281168A>G NCBI36
NG_033888.1:g.19710A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1001A>G (DGKE) MANE Select ENSP00000284061.3:p.Gln334Arg
ENST00000648772.1:c.*313+3135T>C (TRIM25) ENSP00000498158.1:n.*313+3135T>C
ENST00000284061.7:c.1001A>G (DGKE) ENSP00000284061.3:p.Gln334Arg
ENST00000572944.1:c.831A>G (DGKE)
NM_003647.2:c.1001A>G (DGKE) NP_003638.1:p.Gln334Arg
XM_011525394.1:c.1055A>G (DGKE) XP_011523696.1:p.Gln352Arg
XM_011525395.1:c.1055A>G (DGKE) XP_011523697.1:p.Gln352Arg
XM_011525396.1:c.1055A>G (DGKE) XP_011523698.1:p.Gln352Arg
XM_011525397.1:c.1055A>G (DGKE) XP_011523699.1:p.Gln352Arg
XM_011525398.1:c.545A>G (DGKE) XP_011523700.1:p.Gln182Arg
XR_934581.1:n.1154A>G (DGKE)
XM_011525394.3:c.1055A>G (DGKE) XP_011523696.1:p.Gln352Arg
XM_011525395.2:c.1055A>G (DGKE) XP_011523697.1:p.Gln352Arg
XM_011525396.2:c.1055A>G (DGKE) XP_011523698.1:p.Gln352Arg
XM_017025243.2:c.1373A>G (DGKE) XP_016880732.1:p.Gln458Arg
XM_017025244.2:c.1055A>G (DGKE) XP_016880733.1:p.Gln352Arg
XR_001752670.2:n.1559A>G (DGKE)
XR_001752671.1:n.1166A>G (DGKE)
XR_001752672.1:n.1167A>G (DGKE)
XR_002958079.1:n.1165A>G (DGKE)
NM_003647.3:c.1001A>G (DGKE) MANE Select NP_003638.1:p.Gln334Arg