Canonical Allele Identifier: CA399926711

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845718C>G , CM000679.2:g.56845718C>G GRCh38
NC_000017.10:g.54923079C>G , CM000679.1:g.54923079C>G GRCh37
NC_000017.9:g.52278078C>G NCBI36
NG_033888.1:g.16620C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.653C>G (DGKE) MANE Select ENSP00000284061.3:p.Thr218Ser
ENST00000648772.1:c.*314-1928G>C (TRIM25) ENSP00000498158.1:n.*314-1928G>C
ENST00000284061.7:c.653C>G (DGKE) ENSP00000284061.3:p.Thr218Ser
ENST00000571084.1:n.189C>G (DGKE)
ENST00000572944.1:c.483C>G (DGKE)
ENST00000576869.5:n.801C>G (DGKE)
NM_003647.2:c.653C>G (DGKE) NP_003638.1:p.Thr218Ser
XM_011525394.1:c.707C>G (DGKE) XP_011523696.1:p.Thr236Ser
XM_011525395.1:c.707C>G (DGKE) XP_011523697.1:p.Thr236Ser
XM_011525396.1:c.707C>G (DGKE) XP_011523698.1:p.Thr236Ser
XM_011525397.1:c.707C>G (DGKE) XP_011523699.1:p.Thr236Ser
XM_011525398.1:c.197C>G (DGKE) XP_011523700.1:p.Thr66Ser
XR_934581.1:n.806C>G (DGKE)
XM_011525394.3:c.707C>G (DGKE) XP_011523696.1:p.Thr236Ser
XM_011525395.2:c.707C>G (DGKE) XP_011523697.1:p.Thr236Ser
XM_011525396.2:c.707C>G (DGKE) XP_011523698.1:p.Thr236Ser
XM_017025243.2:c.653C>G (DGKE) XP_016880732.1:p.Thr218Ser
XM_017025244.2:c.707C>G (DGKE) XP_016880733.1:p.Thr236Ser
XR_001752670.2:n.839C>G (DGKE)
XR_001752671.1:n.818C>G (DGKE)
XR_001752672.1:n.819C>G (DGKE)
XR_002958079.1:n.817C>G (DGKE)
NM_003647.3:c.653C>G (DGKE) MANE Select NP_003638.1:p.Thr218Ser