Canonical Allele Identifier: CA399905780

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56856606C>A , CM000679.2:g.56856606C>A GRCh38
NC_000017.10:g.54933967C>A , CM000679.1:g.54933967C>A GRCh37
NC_000017.9:g.52288966C>A NCBI36
NG_033888.1:g.27508C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682766.1:c.1364-1496G>T (TRIM25) ENSP00000507876.1:n.1364-1496G>T
ENST00000284061.8:c.1193C>A (DGKE) MANE Select ENSP00000284061.3:p.Ser398Tyr
ENST00000648772.1:c.1364-1496G>T (TRIM25) ENSP00000498158.1:n.1364-1496G>T
ENST00000284061.7:c.1193C>A (DGKE) ENSP00000284061.3:p.Ser398Tyr
ENST00000572944.1:c.1023C>A (DGKE)
NM_003647.2:c.1193C>A (DGKE) NP_003638.1:p.Ser398Tyr
XM_011525394.1:c.1247C>A (DGKE) XP_011523696.1:p.Ser416Tyr
XM_011525395.1:c.1247C>A (DGKE) XP_011523697.1:p.Ser416Tyr
XM_011525396.1:c.1247C>A (DGKE) XP_011523698.1:p.Ser416Tyr
XM_011525397.1:c.1247C>A (DGKE) XP_011523699.1:p.Ser416Tyr
XM_011525398.1:c.737C>A (DGKE) XP_011523700.1:p.Ser246Tyr
XR_934581.1:n.1346C>A (DGKE)
XM_011525394.3:c.1247C>A (DGKE) XP_011523696.1:p.Ser416Tyr
XM_011525395.2:c.1247C>A (DGKE) XP_011523697.1:p.Ser416Tyr
XM_011525396.2:c.1247C>A (DGKE) XP_011523698.1:p.Ser416Tyr
XM_017025243.2:c.1565C>A (DGKE) XP_016880732.1:p.Ser522Tyr
XM_017025244.2:c.1247C>A (DGKE) XP_016880733.1:p.Ser416Tyr
XR_001752670.2:n.1751C>A (DGKE)
XR_001752671.1:n.1358C>A (DGKE)
XR_001752672.1:n.1359C>A (DGKE)
XR_002958079.1:n.1357C>A (DGKE)
NM_003647.3:c.1193C>A (DGKE) MANE Select NP_003638.1:p.Ser398Tyr