Canonical Allele Identifier: CA2266993814

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56846034T= , CM000679.2:g.56846034T= GRCh38
NC_000017.10:g.54923395T= , CM000679.1:g.54923395T= GRCh37
NC_000017.9:g.52278394T= NCBI36
NG_033888.1:g.16936T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.744+225T= (DGKE) MANE Select ENSP00000284061.3:n.744+225T=
ENST00000648772.1:c.*314-2244A= (TRIM25) ENSP00000498158.1:n.*314-2244A=
ENST00000284061.7:c.744+225T= (DGKE) ENSP00000284061.3:n.744+225T=
ENST00000571084.1:n.505T= (DGKE)
ENST00000572944.1:c.574+225T= (DGKE)
ENST00000576869.5:n.892+225T= (DGKE)
NM_003647.2:c.744+225T= (DGKE) NP_003638.1:n.744+225T=
XM_011525394.1:c.798+225T= (DGKE) XP_011523696.1:n.798+225T=
XM_011525395.1:c.798+225T= (DGKE) XP_011523697.1:n.798+225T=
XM_011525396.1:c.798+225T= (DGKE) XP_011523698.1:n.798+225T=
XM_011525397.1:c.798+225T= (DGKE) XP_011523699.1:n.798+225T=
XM_011525398.1:c.288+225T= (DGKE) XP_011523700.1:n.288+225T=
XR_934581.1:n.897+225T= (DGKE)
XM_011525394.3:c.798+225T= (DGKE) XP_011523696.1:n.798+225T=
XM_011525395.2:c.798+225T= (DGKE) XP_011523697.1:n.798+225T=
XM_011525396.2:c.798+225T= (DGKE) XP_011523698.1:n.798+225T=
XM_017025243.2:c.744+225T= (DGKE) XP_016880732.1:n.744+225T=
XM_017025244.2:c.798+225T= (DGKE) XP_016880733.1:n.798+225T=
XR_001752670.2:n.930+225T= (DGKE)
XR_001752671.1:n.909+225T= (DGKE)
XR_001752672.1:n.910+225T= (DGKE)
XR_002958079.1:n.908+225T= (DGKE)
NM_003647.3:c.744+225T= (DGKE) MANE Select NP_003638.1:n.744+225T=