Canonical Allele Identifier: CA399926007

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56844057T>G , CM000679.2:g.56844057T>G GRCh38
NC_000017.10:g.54921418T>G , CM000679.1:g.54921418T>G GRCh37
NC_000017.9:g.52276417T>G NCBI36
NG_033888.1:g.14959T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.503T>G (DGKE) MANE Select ENSP00000284061.3:p.Met168Arg
ENST00000648772.1:c.*314-267A>C (TRIM25) ENSP00000498158.1:n.*314-267A>C
ENST00000284061.7:c.503T>G (DGKE) ENSP00000284061.3:p.Met168Arg
ENST00000571084.1:n.39T>G (DGKE)
ENST00000572944.1:c.333T>G (DGKE)
ENST00000576869.5:n.651T>G (DGKE)
NM_003647.2:c.503T>G (DGKE) NP_003638.1:p.Met168Arg
XM_011525394.1:c.557T>G (DGKE) XP_011523696.1:p.Met186Arg
XM_011525395.1:c.557T>G (DGKE) XP_011523697.1:p.Met186Arg
XM_011525396.1:c.557T>G (DGKE) XP_011523698.1:p.Met186Arg
XM_011525397.1:c.557T>G (DGKE) XP_011523699.1:p.Met186Arg
XM_011525398.1:c.47T>G (DGKE) XP_011523700.1:p.Met16Arg
XR_934581.1:n.656T>G (DGKE)
XM_011525394.3:c.557T>G (DGKE) XP_011523696.1:p.Met186Arg
XM_011525395.2:c.557T>G (DGKE) XP_011523697.1:p.Met186Arg
XM_011525396.2:c.557T>G (DGKE) XP_011523698.1:p.Met186Arg
XM_017025243.2:c.503T>G (DGKE) XP_016880732.1:p.Met168Arg
XM_017025244.2:c.557T>G (DGKE) XP_016880733.1:p.Met186Arg
XR_001752670.2:n.689T>G (DGKE)
XR_001752671.1:n.668T>G (DGKE)
XR_001752672.1:n.669T>G (DGKE)
XR_002958079.1:n.667T>G (DGKE)
NM_003647.3:c.503T>G (DGKE) MANE Select NP_003638.1:p.Met168Arg