Canonical Allele Identifier: CA399927664

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848701A>C , CM000679.2:g.56848701A>C GRCh38
NC_000017.10:g.54926062A>C , CM000679.1:g.54926062A>C GRCh37
NC_000017.9:g.52281061A>C NCBI36
NG_033888.1:g.19603A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.894A>C (DGKE) MANE Select ENSP00000284061.3:p.Gln298His
ENST00000648772.1:c.*313+3242T>G (TRIM25) ENSP00000498158.1:n.*313+3242T>G
ENST00000284061.7:c.894A>C (DGKE) ENSP00000284061.3:p.Gln298His
ENST00000572944.1:c.724A>C (DGKE)
NM_003647.2:c.894A>C (DGKE) NP_003638.1:p.Gln298His
XM_011525394.1:c.948A>C (DGKE) XP_011523696.1:p.Gln316His
XM_011525395.1:c.948A>C (DGKE) XP_011523697.1:p.Gln316His
XM_011525396.1:c.948A>C (DGKE) XP_011523698.1:p.Gln316His
XM_011525397.1:c.948A>C (DGKE) XP_011523699.1:p.Gln316His
XM_011525398.1:c.438A>C (DGKE) XP_011523700.1:p.Gln146His
XR_934581.1:n.1047A>C (DGKE)
XM_011525394.3:c.948A>C (DGKE) XP_011523696.1:p.Gln316His
XM_011525395.2:c.948A>C (DGKE) XP_011523697.1:p.Gln316His
XM_011525396.2:c.948A>C (DGKE) XP_011523698.1:p.Gln316His
XM_017025243.2:c.1266A>C (DGKE) XP_016880732.1:p.Gln422His
XM_017025244.2:c.948A>C (DGKE) XP_016880733.1:p.Gln316His
XR_001752670.2:n.1452A>C (DGKE)
XR_001752671.1:n.1059A>C (DGKE)
XR_001752672.1:n.1060A>C (DGKE)
XR_002958079.1:n.1058A>C (DGKE)
NM_003647.3:c.894A>C (DGKE) MANE Select NP_003638.1:p.Gln298His