Canonical Allele Identifier: CA1584036725

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371234A= , CM000667.2:g.134371234A= GRCh38
NC_000005.9:g.133706925A= , CM000667.1:g.133706925A= GRCh37
NC_000005.8:g.133734824A= NCBI36
NG_042179.2:g.4814T=
NG_046936.1:g.5059A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507277.2:c.-362A= (UBE2B) ENSP00000425137.2:n.-362A=
ENST00000265339.6:c.-362A= (UBE2B) ENSP00000265339.2:n.-362A=
NM_003337.3:c.-362A= (UBE2B) NP_003328.1:n.-362A=
XM_011543441.1:c.-224+164T= (CDKL3) XP_011541743.1:n.-224+164T=
XM_017009544.2:c.-868T= (CDKL3) XP_016865033.1:n.-868T=
XM_017009545.2:c.-673T= (CDKL3) XP_016865034.1:n.-673T=
XM_024446086.1:c.-258T= (CDKL3) XP_024301854.1:n.-258T=
XM_024446093.1:c.227+164T= (CDKL3) XP_024301861.1:n.227+164T=
XM_024446096.1:c.-639T= (CDKL3) XP_024301864.1:n.-639T=
XM_024446097.1:c.-660T= (CDKL3) XP_024301865.1:n.-660T=
XM_024446099.1:c.-439+164T= (CDKL3) XP_024301867.1:n.-439+164T=
XM_024446100.1:c.-460T= (CDKL3) XP_024301868.1:n.-460T=
XM_024446101.1:c.-250T= (CDKL3) XP_024301869.1:n.-250T=
XM_024446103.1:c.-460T= (CDKL3) XP_024301871.1:n.-460T=