Canonical Allele Identifier: CA2266995110

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848760A= , CM000679.2:g.56848760A= GRCh38
NC_000017.10:g.54926121A= , CM000679.1:g.54926121A= GRCh37
NC_000017.9:g.52281120A= NCBI36
NG_033888.1:g.19662A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.953A= (DGKE) MANE Select ENSP00000284061.3:p.Asn318=
ENST00000648772.1:c.*313+3183T= (TRIM25) ENSP00000498158.1:n.*313+3183T=
ENST00000284061.7:c.953A= (DGKE) ENSP00000284061.3:p.Asn318=
ENST00000572944.1:c.783A= (DGKE)
NM_003647.2:c.953A= (DGKE) NP_003638.1:p.Asn318=
XM_011525394.1:c.1007A= (DGKE) XP_011523696.1:p.Asn336=
XM_011525395.1:c.1007A= (DGKE) XP_011523697.1:p.Asn336=
XM_011525396.1:c.1007A= (DGKE) XP_011523698.1:p.Asn336=
XM_011525397.1:c.1007A= (DGKE) XP_011523699.1:p.Asn336=
XM_011525398.1:c.497A= (DGKE) XP_011523700.1:p.Asn166=
XR_934581.1:n.1106A= (DGKE)
XM_011525394.3:c.1007A= (DGKE) XP_011523696.1:p.Asn336=
XM_011525395.2:c.1007A= (DGKE) XP_011523697.1:p.Asn336=
XM_011525396.2:c.1007A= (DGKE) XP_011523698.1:p.Asn336=
XM_017025243.2:c.1325A= (DGKE) XP_016880732.1:p.Asn442=
XM_017025244.2:c.1007A= (DGKE) XP_016880733.1:p.Asn336=
XR_001752670.2:n.1511A= (DGKE)
XR_001752671.1:n.1118A= (DGKE)
XR_001752672.1:n.1119A= (DGKE)
XR_002958079.1:n.1117A= (DGKE)
NM_003647.3:c.953A= (DGKE) MANE Select NP_003638.1:p.Asn318=