Canonical Allele Identifier: CA399905480

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56856514A>C , CM000679.2:g.56856514A>C GRCh38
NC_000017.10:g.54933875A>C , CM000679.1:g.54933875A>C GRCh37
NC_000017.9:g.52288874A>C NCBI36
NG_033888.1:g.27416A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682766.1:c.1364-1404T>G (TRIM25) ENSP00000507876.1:n.1364-1404T>G
ENST00000284061.8:c.1101A>C (DGKE) MANE Select ENSP00000284061.3:p.Glu367Asp
ENST00000648772.1:c.1364-1404T>G (TRIM25) ENSP00000498158.1:n.1364-1404T>G
ENST00000284061.7:c.1101A>C (DGKE) ENSP00000284061.3:p.Glu367Asp
ENST00000572944.1:c.931A>C (DGKE)
NM_003647.2:c.1101A>C (DGKE) NP_003638.1:p.Glu367Asp
XM_011525394.1:c.1155A>C (DGKE) XP_011523696.1:p.Glu385Asp
XM_011525395.1:c.1155A>C (DGKE) XP_011523697.1:p.Glu385Asp
XM_011525396.1:c.1155A>C (DGKE) XP_011523698.1:p.Glu385Asp
XM_011525397.1:c.1155A>C (DGKE) XP_011523699.1:p.Glu385Asp
XM_011525398.1:c.645A>C (DGKE) XP_011523700.1:p.Glu215Asp
XR_934581.1:n.1254A>C (DGKE)
XM_011525394.3:c.1155A>C (DGKE) XP_011523696.1:p.Glu385Asp
XM_011525395.2:c.1155A>C (DGKE) XP_011523697.1:p.Glu385Asp
XM_011525396.2:c.1155A>C (DGKE) XP_011523698.1:p.Glu385Asp
XM_017025243.2:c.1473A>C (DGKE) XP_016880732.1:p.Glu491Asp
XM_017025244.2:c.1155A>C (DGKE) XP_016880733.1:p.Glu385Asp
XR_001752670.2:n.1659A>C (DGKE)
XR_001752671.1:n.1266A>C (DGKE)
XR_001752672.1:n.1267A>C (DGKE)
XR_002958079.1:n.1265A>C (DGKE)
NM_003647.3:c.1101A>C (DGKE) MANE Select NP_003638.1:p.Glu367Asp