Canonical Allele Identifier: CA2266995132

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56848820A= , CM000679.2:g.56848820A= GRCh38
NC_000017.10:g.54926181A= , CM000679.1:g.54926181A= GRCh37
NC_000017.9:g.52281180A= NCBI36
NG_033888.1:g.19722A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284061.8:c.1013A= (DGKE) MANE Select ENSP00000284061.3:p.Asn338=
ENST00000648772.1:c.*313+3123T= (TRIM25) ENSP00000498158.1:n.*313+3123T=
ENST00000284061.7:c.1013A= (DGKE) ENSP00000284061.3:p.Asn338=
ENST00000572944.1:c.843A= (DGKE)
NM_003647.2:c.1013A= (DGKE) NP_003638.1:p.Asn338=
XM_011525394.1:c.1067A= (DGKE) XP_011523696.1:p.Asn356=
XM_011525395.1:c.1067A= (DGKE) XP_011523697.1:p.Asn356=
XM_011525396.1:c.1067A= (DGKE) XP_011523698.1:p.Asn356=
XM_011525397.1:c.1067A= (DGKE) XP_011523699.1:p.Asn356=
XM_011525398.1:c.557A= (DGKE) XP_011523700.1:p.Asn186=
XR_934581.1:n.1166A= (DGKE)
XM_011525394.3:c.1067A= (DGKE) XP_011523696.1:p.Asn356=
XM_011525395.2:c.1067A= (DGKE) XP_011523697.1:p.Asn356=
XM_011525396.2:c.1067A= (DGKE) XP_011523698.1:p.Asn356=
XM_017025243.2:c.1385A= (DGKE) XP_016880732.1:p.Asn462=
XM_017025244.2:c.1067A= (DGKE) XP_016880733.1:p.Asn356=
XR_001752670.2:n.1571A= (DGKE)
XR_001752671.1:n.1178A= (DGKE)
XR_001752672.1:n.1179A= (DGKE)
XR_002958079.1:n.1177A= (DGKE)
NM_003647.3:c.1013A= (DGKE) MANE Select NP_003638.1:p.Asn338=