Canonical Allele Identifier: CA269957
Gene: CUL3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 100518
ClinVar RCV Id: RCV000128489
dbSNP Id: rs199469649

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503850A>C , CM000664.2:g.224503850A>C GRCh38
NC_000002.11:g.225368567A>C , CM000664.1:g.225368567A>C GRCh37
NC_000002.10:g.225076811A>C NCBI36
NG_032169.1:g.86548T>G

Transcript Alleles

HGVS Amino-acid change
NM_001257197.1:c.1009-28T>G VV NP_001244126.1:p.=
NM_001257198.1:c.1225-28T>G VV NP_001244127.1:p.=
NM_003590.4:c.1207-28T>G VV NP_003581.1:p.=
XM_006712800.2:c.1174-28T>G XP_006712863.2:p.=
XM_011511994.1:c.1060-28T>G XP_011510296.1:p.=
XM_011511995.1:c.1165-28T>G XP_011510297.1:p.=
XM_011511996.1:c.1015-28T>G XP_011510298.1:p.=
XM_011511997.1:c.907-28T>G XP_011510299.1:p.=
XM_011511994.3:c.1060-28T>G XP_011510296.1:p.=
XM_011511996.2:c.1015-28T>G XP_011510298.1:p.=
NM_003590.5:c.1207-28T>G VV MANE Preferred NP_003581.1:p.=
ENST00000264414.8:c.1207-28T>G ENSP00000264414.4:p.=
ENST00000344951.8:c.1009-28T>G ENSP00000343601.4:p.=
ENST00000409096.5:c.1135-28T>G ENSP00000387200.1:p.=
ENST00000409777.5:c.1135-28T>G ENSP00000386525.1:p.=
ENST00000481135.1:n.475T>G
ENST00000617432.4:c.-70-28T>G ENSP00000477851.1:p.=