Canonical Allele Identifier: CA2663372733
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224504222_224504223del , CM000664.2:g.224504222_224504223del GRCh38
NC_000002.11:g.225368939_225368940del , CM000664.1:g.225368939_225368940del GRCh37
NC_000002.10:g.225077183_225077184del NCBI36
NG_032169.1:g.86176_86177del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1207-400_1207-399del MANE Select ENSP00000264414.4:n.1207-400_1207-399del
ENST00000264414.8:c.1207-400_1207-399del ENSP00000264414.4:n.1207-400_1207-399del
ENST00000344951.8:c.1009-400_1009-399del ENSP00000343601.4:n.1009-400_1009-399del
ENST00000409096.5:c.1135-400_1135-399del ENSP00000387200.1:n.1135-400_1135-399del
ENST00000409777.5:c.1135-400_1135-399del ENSP00000386525.1:n.1135-400_1135-399del
ENST00000481135.1:n.103_104del
ENST00000617432.4:c.-70-400_-70-399del ENSP00000477851.1:n.-70-400_-70-399del
NM_001257197.1:c.1009-400_1009-399del NP_001244126.1:n.1009-400_1009-399del
NM_001257198.1:c.1225-400_1225-399del NP_001244127.1:n.1225-400_1225-399del
NM_003590.4:c.1207-400_1207-399del NP_003581.1:n.1207-400_1207-399del
XM_006712800.2:c.1174-400_1174-399del XP_006712863.2:n.1174-400_1174-399del
XM_011511994.1:c.1060-400_1060-399del XP_011510296.1:n.1060-400_1060-399del
XM_011511995.1:c.1165-400_1165-399del XP_011510297.1:n.1165-400_1165-399del
XM_011511996.1:c.1015-400_1015-399del XP_011510298.1:n.1015-400_1015-399del
XM_011511997.1:c.907-400_907-399del XP_011510299.1:n.907-400_907-399del
XM_011511994.3:c.1060-400_1060-399del XP_011510296.1:n.1060-400_1060-399del
XM_011511996.2:c.1015-400_1015-399del XP_011510298.1:n.1015-400_1015-399del
NM_003590.5:c.1207-400_1207-399del MANE Select NP_003581.1:n.1207-400_1207-399del
NM_001257198.2:c.1225-400_1225-399del NP_001244127.1:n.1225-400_1225-399del
NM_001257197.2:c.1009-400_1009-399del NP_001244126.1:n.1009-400_1009-399del