Canonical Allele Identifier: CA399926669

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845703T>C , CM000679.2:g.56845703T>C GRCh38
NC_000017.10:g.54923064T>C , CM000679.1:g.54923064T>C GRCh37
NC_000017.9:g.52278063T>C NCBI36
NG_033888.1:g.16605T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.638T>C (DGKE) MANE Select ENSP00000284061.3:p.Leu213Pro
ENST00000648772.1:c.*314-1913A>G (TRIM25) ENSP00000498158.1:n.*314-1913A>G
ENST00000284061.7:c.638T>C (DGKE) ENSP00000284061.3:p.Leu213Pro
ENST00000571084.1:n.174T>C (DGKE)
ENST00000572944.1:c.468T>C (DGKE)
ENST00000576869.5:n.786T>C (DGKE)
NM_003647.2:c.638T>C (DGKE) NP_003638.1:p.Leu213Pro
XM_011525394.1:c.692T>C (DGKE) XP_011523696.1:p.Leu231Pro
XM_011525395.1:c.692T>C (DGKE) XP_011523697.1:p.Leu231Pro
XM_011525396.1:c.692T>C (DGKE) XP_011523698.1:p.Leu231Pro
XM_011525397.1:c.692T>C (DGKE) XP_011523699.1:p.Leu231Pro
XM_011525398.1:c.182T>C (DGKE) XP_011523700.1:p.Leu61Pro
XR_934581.1:n.791T>C (DGKE)
XM_011525394.3:c.692T>C (DGKE) XP_011523696.1:p.Leu231Pro
XM_011525395.2:c.692T>C (DGKE) XP_011523697.1:p.Leu231Pro
XM_011525396.2:c.692T>C (DGKE) XP_011523698.1:p.Leu231Pro
XM_017025243.2:c.638T>C (DGKE) XP_016880732.1:p.Leu213Pro
XM_017025244.2:c.692T>C (DGKE) XP_016880733.1:p.Leu231Pro
XR_001752670.2:n.824T>C (DGKE)
XR_001752671.1:n.803T>C (DGKE)
XR_001752672.1:n.804T>C (DGKE)
XR_002958079.1:n.802T>C (DGKE)
NM_003647.3:c.638T>C (DGKE) MANE Select NP_003638.1:p.Leu213Pro