Canonical Allele Identifier: CA350827118
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503694A>C , CM000664.2:g.224503694A>C GRCh38
NC_000002.11:g.225368411A>C , CM000664.1:g.225368411A>C GRCh37
NC_000002.10:g.225076655A>C NCBI36
NG_032169.1:g.86704T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1335T>G MANE Select ENSP00000264414.4:p.Ser445Arg
ENST00000264414.8:c.1335T>G ENSP00000264414.4:p.Ser445Arg
ENST00000344951.8:c.1137T>G ENSP00000343601.4:p.Ser379Arg
ENST00000409096.5:c.1263T>G ENSP00000387200.1:p.Ser421Arg
ENST00000409777.5:c.1263T>G ENSP00000386525.1:p.Ser421Arg
ENST00000481135.1:n.631T>G
ENST00000617432.4:c.59T>G ENSP00000477851.1:p.Val20Gly
NM_001257197.1:c.1137T>G NP_001244126.1:p.Ser379Arg
NM_001257198.1:c.1353T>G NP_001244127.1:p.Ser451Arg
NM_003590.4:c.1335T>G NP_003581.1:p.Ser445Arg
XM_006712800.2:c.1302T>G XP_006712863.2:p.Ser434Arg
XM_011511994.1:c.1188T>G XP_011510296.1:p.Ser396Arg
XM_011511995.1:c.1293T>G XP_011510297.1:p.Ser431Arg
XM_011511996.1:c.1143T>G XP_011510298.1:p.Ser381Arg
XM_011511997.1:c.1035T>G XP_011510299.1:p.Ser345Arg
XM_011511994.3:c.1188T>G XP_011510296.1:p.Ser396Arg
XM_011511996.2:c.1143T>G XP_011510298.1:p.Ser381Arg
NM_003590.5:c.1335T>G MANE Select NP_003581.1:p.Ser445Arg
NM_001257198.2:c.1353T>G NP_001244127.1:p.Ser451Arg
NM_001257197.2:c.1137T>G NP_001244126.1:p.Ser379Arg