Canonical Allele Identifier: CA2663372735
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224504226_224504236del , CM000664.2:g.224504226_224504236del GRCh38
NC_000002.11:g.225368943_225368953del , CM000664.1:g.225368943_225368953del GRCh37
NC_000002.10:g.225077187_225077197del NCBI36
NG_032169.1:g.86162_86172del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1207-414_1207-404del MANE Select ENSP00000264414.4:n.1207-414_1207-404del
ENST00000264414.8:c.1207-414_1207-404del ENSP00000264414.4:n.1207-414_1207-404del
ENST00000344951.8:c.1009-414_1009-404del ENSP00000343601.4:n.1009-414_1009-404del
ENST00000409096.5:c.1135-414_1135-404del ENSP00000387200.1:n.1135-414_1135-404del
ENST00000409777.5:c.1135-414_1135-404del ENSP00000386525.1:n.1135-414_1135-404del
ENST00000481135.1:n.89_99del
ENST00000617432.4:c.-70-414_-70-404del ENSP00000477851.1:n.-70-414_-70-404del
NM_001257197.1:c.1009-414_1009-404del NP_001244126.1:n.1009-414_1009-404del
NM_001257198.1:c.1225-414_1225-404del NP_001244127.1:n.1225-414_1225-404del
NM_003590.4:c.1207-414_1207-404del NP_003581.1:n.1207-414_1207-404del
XM_006712800.2:c.1174-414_1174-404del XP_006712863.2:n.1174-414_1174-404del
XM_011511994.1:c.1060-414_1060-404del XP_011510296.1:n.1060-414_1060-404del
XM_011511995.1:c.1165-414_1165-404del XP_011510297.1:n.1165-414_1165-404del
XM_011511996.1:c.1015-414_1015-404del XP_011510298.1:n.1015-414_1015-404del
XM_011511997.1:c.907-414_907-404del XP_011510299.1:n.907-414_907-404del
XM_011511994.3:c.1060-414_1060-404del XP_011510296.1:n.1060-414_1060-404del
XM_011511996.2:c.1015-414_1015-404del XP_011510298.1:n.1015-414_1015-404del
NM_003590.5:c.1207-414_1207-404del MANE Select NP_003581.1:n.1207-414_1207-404del
NM_001257198.2:c.1225-414_1225-404del NP_001244127.1:n.1225-414_1225-404del
NM_001257197.2:c.1009-414_1009-404del NP_001244126.1:n.1009-414_1009-404del