Canonical Allele Identifier: CA399927708

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848709A>G , CM000679.2:g.56848709A>G GRCh38
NC_000017.10:g.54926070A>G , CM000679.1:g.54926070A>G GRCh37
NC_000017.9:g.52281069A>G NCBI36
NG_033888.1:g.19611A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.902A>G (DGKE) MANE Select ENSP00000284061.3:p.Tyr301Cys
ENST00000648772.1:c.*313+3234T>C (TRIM25) ENSP00000498158.1:n.*313+3234T>C
ENST00000284061.7:c.902A>G (DGKE) ENSP00000284061.3:p.Tyr301Cys
ENST00000572944.1:c.732A>G (DGKE)
NM_003647.2:c.902A>G (DGKE) NP_003638.1:p.Tyr301Cys
XM_011525394.1:c.956A>G (DGKE) XP_011523696.1:p.Tyr319Cys
XM_011525395.1:c.956A>G (DGKE) XP_011523697.1:p.Tyr319Cys
XM_011525396.1:c.956A>G (DGKE) XP_011523698.1:p.Tyr319Cys
XM_011525397.1:c.956A>G (DGKE) XP_011523699.1:p.Tyr319Cys
XM_011525398.1:c.446A>G (DGKE) XP_011523700.1:p.Tyr149Cys
XR_934581.1:n.1055A>G (DGKE)
XM_011525394.3:c.956A>G (DGKE) XP_011523696.1:p.Tyr319Cys
XM_011525395.2:c.956A>G (DGKE) XP_011523697.1:p.Tyr319Cys
XM_011525396.2:c.956A>G (DGKE) XP_011523698.1:p.Tyr319Cys
XM_017025243.2:c.1274A>G (DGKE) XP_016880732.1:p.Tyr425Cys
XM_017025244.2:c.956A>G (DGKE) XP_016880733.1:p.Tyr319Cys
XR_001752670.2:n.1460A>G (DGKE)
XR_001752671.1:n.1067A>G (DGKE)
XR_001752672.1:n.1068A>G (DGKE)
XR_002958079.1:n.1066A>G (DGKE)
NM_003647.3:c.902A>G (DGKE) MANE Select NP_003638.1:p.Tyr301Cys