Canonical Allele Identifier: CA1331555923
Gene: CUL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503662G= , CM000664.2:g.224503662G= GRCh38
NC_000002.11:g.225368379G= , CM000664.1:g.225368379G= GRCh37
NC_000002.10:g.225076623G= NCBI36
NG_032169.1:g.86736C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1367C= MANE Select ENSP00000264414.4:p.Ser456=
ENST00000264414.8:c.1367C= ENSP00000264414.4:p.Ser456=
ENST00000344951.8:c.1169C= ENSP00000343601.4:p.Ser390=
ENST00000409096.5:c.1295C= ENSP00000387200.1:p.Ser432=
ENST00000409777.5:c.1295C= ENSP00000386525.1:p.Ser432=
ENST00000481135.1:n.663C=
ENST00000617432.4:c.89C= ENSP00000477851.1:p.Ser30=
NM_001257197.1:c.1169C= NP_001244126.1:p.Ser390=
NM_001257198.1:c.1385C= NP_001244127.1:p.Ser462=
NM_003590.4:c.1367C= NP_003581.1:p.Ser456=
XM_006712800.2:c.1334C= XP_006712863.2:p.Ser445=
XM_011511994.1:c.1220C= XP_011510296.1:p.Ser407=
XM_011511995.1:c.1325C= XP_011510297.1:p.Ser442=
XM_011511996.1:c.1175C= XP_011510298.1:p.Ser392=
XM_011511997.1:c.1067C= XP_011510299.1:p.Ser356=
XM_011511994.3:c.1220C= XP_011510296.1:p.Ser407=
XM_011511996.2:c.1175C= XP_011510298.1:p.Ser392=
NM_003590.5:c.1367C= MANE Select NP_003581.1:p.Ser456=
NM_001257198.2:c.1385C= NP_001244127.1:p.Ser462=
NM_001257197.2:c.1169C= NP_001244126.1:p.Ser390=