Canonical Allele Identifier: CA350827266
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503710A>G , CM000664.2:g.224503710A>G GRCh38
NC_000002.11:g.225368427A>G , CM000664.1:g.225368427A>G GRCh37
NC_000002.10:g.225076671A>G NCBI36
NG_032169.1:g.86688T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1319T>C MANE Select ENSP00000264414.4:p.Leu440Pro
ENST00000264414.8:c.1319T>C ENSP00000264414.4:p.Leu440Pro
ENST00000344951.8:c.1121T>C ENSP00000343601.4:p.Leu374Pro
ENST00000409096.5:c.1247T>C ENSP00000387200.1:p.Leu416Pro
ENST00000409777.5:c.1247T>C ENSP00000386525.1:p.Leu416Pro
ENST00000481135.1:n.615T>C
ENST00000617432.4:c.43T>C ENSP00000477851.1:p.Phe15Leu
NM_001257197.1:c.1121T>C NP_001244126.1:p.Leu374Pro
NM_001257198.1:c.1337T>C NP_001244127.1:p.Leu446Pro
NM_003590.4:c.1319T>C NP_003581.1:p.Leu440Pro
XM_006712800.2:c.1286T>C XP_006712863.2:p.Leu429Pro
XM_011511994.1:c.1172T>C XP_011510296.1:p.Leu391Pro
XM_011511995.1:c.1277T>C XP_011510297.1:p.Leu426Pro
XM_011511996.1:c.1127T>C XP_011510298.1:p.Leu376Pro
XM_011511997.1:c.1019T>C XP_011510299.1:p.Leu340Pro
XM_011511994.3:c.1172T>C XP_011510296.1:p.Leu391Pro
XM_011511996.2:c.1127T>C XP_011510298.1:p.Leu376Pro
NM_003590.5:c.1319T>C MANE Select NP_003581.1:p.Leu440Pro
NM_001257198.2:c.1337T>C NP_001244127.1:p.Leu446Pro
NM_001257197.2:c.1121T>C NP_001244126.1:p.Leu374Pro