Canonical Allele Identifier: CA1584036783

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371319C= , CM000667.2:g.134371319C= GRCh38
NC_000005.9:g.133707010C= , CM000667.1:g.133707010C= GRCh37
NC_000005.8:g.133734909C= NCBI36
NG_042179.2:g.4729G=
NG_046936.1:g.5144C=

Transcript Alleles

HGVS Amino-acid change
ENST00000507277.2:c.-277C= (UBE2B) ENSP00000425137.2:n.-277C=
ENST00000265339.6:c.-277C= (UBE2B) ENSP00000265339.2:n.-277C=
NM_003337.3:c.-277C= (UBE2B) NP_003328.1:n.-277C=
XM_011543441.1:c.-224+79G= (CDKL3) XP_011541743.1:n.-224+79G=
XM_017009544.2:c.-953G= (CDKL3) XP_016865033.1:n.-953G=
XM_017009545.2:c.-758G= (CDKL3) XP_016865034.1:n.-758G=
XM_024446086.1:c.-343G= (CDKL3) XP_024301854.1:n.-343G=
XM_024446093.1:c.227+79G= (CDKL3) XP_024301861.1:n.227+79G=
XM_024446096.1:c.-724G= (CDKL3) XP_024301864.1:n.-724G=
XM_024446097.1:c.-745G= (CDKL3) XP_024301865.1:n.-745G=
XM_024446099.1:c.-439+79G= (CDKL3) XP_024301867.1:n.-439+79G=
XM_024446100.1:c.-545G= (CDKL3) XP_024301868.1:n.-545G=
XM_024446101.1:c.-335G= (CDKL3) XP_024301869.1:n.-335G=
XM_024446103.1:c.-545G= (CDKL3) XP_024301871.1:n.-545G=