Canonical Allele Identifier: CA2266992965

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56844054G= , CM000679.2:g.56844054G= GRCh38
NC_000017.10:g.54921415G= , CM000679.1:g.54921415G= GRCh37
NC_000017.9:g.52276414G= NCBI36
NG_033888.1:g.14956G=

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.500G= (DGKE) MANE Select ENSP00000284061.3:p.Cys167=
ENST00000648772.1:c.*314-264C= (TRIM25) ENSP00000498158.1:n.*314-264C=
ENST00000284061.7:c.500G= (DGKE) ENSP00000284061.3:p.Cys167=
ENST00000571084.1:n.36G= (DGKE)
ENST00000572944.1:c.330G= (DGKE)
ENST00000576869.5:n.648G= (DGKE)
NM_003647.2:c.500G= (DGKE) NP_003638.1:p.Cys167=
XM_011525394.1:c.554G= (DGKE) XP_011523696.1:p.Cys185=
XM_011525395.1:c.554G= (DGKE) XP_011523697.1:p.Cys185=
XM_011525396.1:c.554G= (DGKE) XP_011523698.1:p.Cys185=
XM_011525397.1:c.554G= (DGKE) XP_011523699.1:p.Cys185=
XM_011525398.1:c.44G= (DGKE) XP_011523700.1:p.Cys15=
XR_934581.1:n.653G= (DGKE)
XM_011525394.3:c.554G= (DGKE) XP_011523696.1:p.Cys185=
XM_011525395.2:c.554G= (DGKE) XP_011523697.1:p.Cys185=
XM_011525396.2:c.554G= (DGKE) XP_011523698.1:p.Cys185=
XM_017025243.2:c.500G= (DGKE) XP_016880732.1:p.Cys167=
XM_017025244.2:c.554G= (DGKE) XP_016880733.1:p.Cys185=
XR_001752670.2:n.686G= (DGKE)
XR_001752671.1:n.665G= (DGKE)
XR_001752672.1:n.666G= (DGKE)
XR_002958079.1:n.664G= (DGKE)
NM_003647.3:c.500G= (DGKE) MANE Select NP_003638.1:p.Cys167=