Canonical Allele Identifier: CA65917009
Community Standard Title: NM_003590.5(CUL3):c.1636C>T (p.Arg546Ter)
Gene: CUL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224497824G>A , CM000664.2:g.224497824G>A GRCh38
NC_000002.11:g.225362541G>A , CM000664.1:g.225362541G>A GRCh37
NC_000002.10:g.225070785G>A NCBI36
NG_032169.1:g.92574C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003590.5:c.1636C>T MANE Select NP_003581.1:p.Arg546Ter
ENST00000264414.9:c.1636C>T MANE Select ENSP00000264414.4:p.Arg546Ter
NM_001257197.1:c.1438C>T NP_001244126.1:p.Arg480Ter
NM_001257197.2:c.1438C>T NP_001244126.1:p.Arg480Ter
NM_001257198.1:c.1654C>T NP_001244127.1:p.Arg552Ter
NM_001257198.2:c.1654C>T NP_001244127.1:p.Arg552Ter
NM_003590.4:c.1636C>T NP_003581.1:p.Arg546Ter
ENST00000264414.8:c.1636C>T ENSP00000264414.4:p.Arg546Ter
ENST00000344951.8:c.1438C>T ENSP00000343601.4:p.Arg480Ter
ENST00000409096.5:c.1564C>T ENSP00000387200.1:p.Arg522Ter
ENST00000409777.5:c.1564C>T ENSP00000386525.1:p.Arg522Ter
ENST00000487558.1:n.61C>T
ENST00000617432.4:c.358C>T ENSP00000477851.1:p.Arg120Ter
XM_006712800.2:c.1603C>T XP_006712863.2:p.Arg535Ter
XM_011511994.1:c.1489C>T XP_011510296.1:p.Arg497Ter
XM_011511994.3:c.1489C>T XP_011510296.1:p.Arg497Ter
XM_011511995.1:c.1594C>T XP_011510297.1:p.Arg532Ter
XM_011511996.1:c.1444C>T XP_011510298.1:p.Arg482Ter
XM_011511996.2:c.1444C>T XP_011510298.1:p.Arg482Ter
XM_011511997.1:c.1336C>T XP_011510299.1:p.Arg446Ter