Canonical Allele Identifier: CA1584037104

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134371636A= , CM000667.2:g.134371636A= GRCh38
NC_000005.9:g.133707327A= , CM000667.1:g.133707327A= GRCh37
NC_000005.8:g.133735226A= NCBI36
NG_042179.2:g.4412T=
NG_046936.1:g.5461A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000507277.2:c.41A= (UBE2B) ENSP00000425137.2:p.Lys14=
ENST00000265339.7:c.41A= (UBE2B) MANE Select ENSP00000265339.2:p.Lys14=
ENST00000265339.6:c.41A= (UBE2B) ENSP00000265339.2:p.Lys14=
ENST00000504431.1:n.31A= (UBE2B)
ENST00000506787.5:c.38A= (UBE2B) ENSP00000426364.1:p.Lys13=
ENST00000507277.1:c.33A= (UBE2B)
ENST00000510021.5:c.41A= (UBE2B) ENSP00000425237.1:p.Lys14=
ENST00000511807.1:n.135A= (UBE2B)
NM_003337.3:c.41A= (UBE2B) NP_003328.1:p.Lys14=
XM_024446093.1:c.-12T= (CDKL3) XP_024301861.1:n.-12T=
NM_003337.4:c.41A= (UBE2B) MANE Select NP_003328.1:p.Lys14=