Canonical Allele Identifier: CA350827759
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503815T>C , CM000664.2:g.224503815T>C GRCh38
NC_000002.11:g.225368532T>C , CM000664.1:g.225368532T>C GRCh37
NC_000002.10:g.225076776T>C NCBI36
NG_032169.1:g.86583A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1214A>G MANE Select ENSP00000264414.4:p.Glu405Gly
ENST00000264414.8:c.1214A>G ENSP00000264414.4:p.Glu405Gly
ENST00000344951.8:c.1016A>G ENSP00000343601.4:p.Glu339Gly
ENST00000409096.5:c.1142A>G ENSP00000387200.1:p.Glu381Gly
ENST00000409777.5:c.1142A>G ENSP00000386525.1:p.Glu381Gly
ENST00000481135.1:n.510A>G
ENST00000617432.4:c.-63A>G ENSP00000477851.1:n.-63A>G
NM_001257197.1:c.1016A>G NP_001244126.1:p.Glu339Gly
NM_001257198.1:c.1232A>G NP_001244127.1:p.Glu411Gly
NM_003590.4:c.1214A>G NP_003581.1:p.Glu405Gly
XM_006712800.2:c.1181A>G XP_006712863.2:p.Glu394Gly
XM_011511994.1:c.1067A>G XP_011510296.1:p.Glu356Gly
XM_011511995.1:c.1172A>G XP_011510297.1:p.Glu391Gly
XM_011511996.1:c.1022A>G XP_011510298.1:p.Glu341Gly
XM_011511997.1:c.914A>G XP_011510299.1:p.Glu305Gly
XM_011511994.3:c.1067A>G XP_011510296.1:p.Glu356Gly
XM_011511996.2:c.1022A>G XP_011510298.1:p.Glu341Gly
NM_003590.5:c.1214A>G MANE Select NP_003581.1:p.Glu405Gly
NM_001257198.2:c.1232A>G NP_001244127.1:p.Glu411Gly
NM_001257197.2:c.1016A>G NP_001244126.1:p.Glu339Gly