Canonical Allele Identifier: CA350827139
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503696T>G , CM000664.2:g.224503696T>G GRCh38
NC_000002.11:g.225368413T>G , CM000664.1:g.225368413T>G GRCh37
NC_000002.10:g.225076657T>G NCBI36
NG_032169.1:g.86702A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1333A>C MANE Select ENSP00000264414.4:p.Ser445Arg
ENST00000264414.8:c.1333A>C ENSP00000264414.4:p.Ser445Arg
ENST00000344951.8:c.1135A>C ENSP00000343601.4:p.Ser379Arg
ENST00000409096.5:c.1261A>C ENSP00000387200.1:p.Ser421Arg
ENST00000409777.5:c.1261A>C ENSP00000386525.1:p.Ser421Arg
ENST00000481135.1:n.629A>C
ENST00000617432.4:c.57A>C ENSP00000477851.1:p.Lys19Asn
NM_001257197.1:c.1135A>C NP_001244126.1:p.Ser379Arg
NM_001257198.1:c.1351A>C NP_001244127.1:p.Ser451Arg
NM_003590.4:c.1333A>C NP_003581.1:p.Ser445Arg
XM_006712800.2:c.1300A>C XP_006712863.2:p.Ser434Arg
XM_011511994.1:c.1186A>C XP_011510296.1:p.Ser396Arg
XM_011511995.1:c.1291A>C XP_011510297.1:p.Ser431Arg
XM_011511996.1:c.1141A>C XP_011510298.1:p.Ser381Arg
XM_011511997.1:c.1033A>C XP_011510299.1:p.Ser345Arg
XM_011511994.3:c.1186A>C XP_011510296.1:p.Ser396Arg
XM_011511996.2:c.1141A>C XP_011510298.1:p.Ser381Arg
NM_003590.5:c.1333A>C MANE Select NP_003581.1:p.Ser445Arg
NM_001257198.2:c.1351A>C NP_001244127.1:p.Ser451Arg
NM_001257197.2:c.1135A>C NP_001244126.1:p.Ser379Arg