Canonical Allele Identifier: CA1139655021
Gene: CUL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503790del , CM000664.2:g.224503790del GRCh38
NC_000002.11:g.225368507del , CM000664.1:g.225368507del GRCh37
NC_000002.10:g.225076751del NCBI36
NG_032169.1:g.86608del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1239del MANE Select ENSP00000264414.4:p.Asp413GlufsTer?
ENST00000264414.8:c.1239del ENSP00000264414.4:p.Asp413GlufsTer?
ENST00000344951.8:c.1041del ENSP00000343601.4:p.Asp347GlufsTer?
ENST00000409096.5:c.1167del ENSP00000387200.1:p.Asp389GlufsTer?
ENST00000409777.5:c.1167del ENSP00000386525.1:p.Asp389GlufsTer?
ENST00000481135.1:n.535del
ENST00000617432.4:c.-38del ENSP00000477851.1:n.-38del
NM_001257197.1:c.1041del NP_001244126.1:p.Asp347GlufsTer?
NM_001257198.1:c.1257del NP_001244127.1:p.Asp419GlufsTer?
NM_003590.4:c.1239del NP_003581.1:p.Asp413GlufsTer?
XM_006712800.2:c.1206del XP_006712863.2:p.Asp402GlufsTer?
XM_011511994.1:c.1092del XP_011510296.1:p.Asp364GlufsTer?
XM_011511995.1:c.1197del XP_011510297.1:p.Asp399GlufsTer?
XM_011511996.1:c.1047del XP_011510298.1:p.Asp349GlufsTer?
XM_011511997.1:c.939del XP_011510299.1:p.Asp313GlufsTer?
XM_011511994.3:c.1092del XP_011510296.1:p.Asp364GlufsTer?
XM_011511996.2:c.1047del XP_011510298.1:p.Asp349GlufsTer?
NM_003590.5:c.1239del MANE Select NP_003581.1:p.Asp413GlufsTer?
NM_001257198.2:c.1257del NP_001244127.1:p.Asp419GlufsTer?
NM_001257197.2:c.1041del NP_001244126.1:p.Asp347GlufsTer?