Canonical Allele Identifier: CA1584036771

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371304A= , CM000667.2:g.134371304A= GRCh38
NC_000005.9:g.133706995A= , CM000667.1:g.133706995A= GRCh37
NC_000005.8:g.133734894A= NCBI36
NG_042179.2:g.4744T=
NG_046936.1:g.5129A=

Transcript Alleles

HGVS Amino-acid change
ENST00000507277.2:c.-292A= (UBE2B) ENSP00000425137.2:n.-292A=
ENST00000265339.6:c.-292A= (UBE2B) ENSP00000265339.2:n.-292A=
NM_003337.3:c.-292A= (UBE2B) NP_003328.1:n.-292A=
XM_011543441.1:c.-224+94T= (CDKL3) XP_011541743.1:n.-224+94T=
XM_017009544.2:c.-938T= (CDKL3) XP_016865033.1:n.-938T=
XM_017009545.2:c.-743T= (CDKL3) XP_016865034.1:n.-743T=
XM_024446086.1:c.-328T= (CDKL3) XP_024301854.1:n.-328T=
XM_024446093.1:c.227+94T= (CDKL3) XP_024301861.1:n.227+94T=
XM_024446096.1:c.-709T= (CDKL3) XP_024301864.1:n.-709T=
XM_024446097.1:c.-730T= (CDKL3) XP_024301865.1:n.-730T=
XM_024446099.1:c.-439+94T= (CDKL3) XP_024301867.1:n.-439+94T=
XM_024446100.1:c.-530T= (CDKL3) XP_024301868.1:n.-530T=
XM_024446101.1:c.-320T= (CDKL3) XP_024301869.1:n.-320T=
XM_024446103.1:c.-530T= (CDKL3) XP_024301871.1:n.-530T=