Canonical Allele Identifier: CA1331555950
Gene: CUL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503767A= , CM000664.2:g.224503767A= GRCh38
NC_000002.11:g.225368484A= , CM000664.1:g.225368484A= GRCh37
NC_000002.10:g.225076728A= NCBI36
NG_032169.1:g.86631T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264414.9:c.1262T= MANE Select ENSP00000264414.4:p.Phe421=
ENST00000264414.8:c.1262T= ENSP00000264414.4:p.Phe421=
ENST00000344951.8:c.1064T= ENSP00000343601.4:p.Phe355=
ENST00000409096.5:c.1190T= ENSP00000387200.1:p.Phe397=
ENST00000409777.5:c.1190T= ENSP00000386525.1:p.Phe397=
ENST00000481135.1:n.558T=
ENST00000617432.4:c.-15T= ENSP00000477851.1:n.-15T=
NM_001257197.1:c.1064T= NP_001244126.1:p.Phe355=
NM_001257198.1:c.1280T= NP_001244127.1:p.Phe427=
NM_003590.4:c.1262T= NP_003581.1:p.Phe421=
XM_006712800.2:c.1229T= XP_006712863.2:p.Phe410=
XM_011511994.1:c.1115T= XP_011510296.1:p.Phe372=
XM_011511995.1:c.1220T= XP_011510297.1:p.Phe407=
XM_011511996.1:c.1070T= XP_011510298.1:p.Phe357=
XM_011511997.1:c.962T= XP_011510299.1:p.Phe321=
XM_011511994.3:c.1115T= XP_011510296.1:p.Phe372=
XM_011511996.2:c.1070T= XP_011510298.1:p.Phe357=
NM_003590.5:c.1262T= MANE Select NP_003581.1:p.Phe421=
NM_001257198.2:c.1280T= NP_001244127.1:p.Phe427=
NM_001257197.2:c.1064T= NP_001244126.1:p.Phe355=