Canonical Allele Identifier: CA2663372601
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503986_224503987dup , CM000664.2:g.224503986_224503987dup GRCh38
NC_000002.11:g.225368703_225368704dup , CM000664.1:g.225368703_225368704dup GRCh37
NC_000002.10:g.225076947_225076948dup NCBI36
NG_032169.1:g.86415_86416dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1207-161_1207-160dup MANE Select ENSP00000264414.4:n.1207-161_1207-160dup
ENST00000264414.8:c.1207-161_1207-160dup ENSP00000264414.4:n.1207-161_1207-160dup
ENST00000344951.8:c.1009-161_1009-160dup ENSP00000343601.4:n.1009-161_1009-160dup
ENST00000409096.5:c.1135-161_1135-160dup ENSP00000387200.1:n.1135-161_1135-160dup
ENST00000409777.5:c.1135-161_1135-160dup ENSP00000386525.1:n.1135-161_1135-160dup
ENST00000481135.1:n.342_343dup
ENST00000617432.4:c.-70-161_-70-160dup ENSP00000477851.1:n.-70-161_-70-160dup
NM_001257197.1:c.1009-161_1009-160dup NP_001244126.1:n.1009-161_1009-160dup
NM_001257198.1:c.1225-161_1225-160dup NP_001244127.1:n.1225-161_1225-160dup
NM_003590.4:c.1207-161_1207-160dup NP_003581.1:n.1207-161_1207-160dup
XM_006712800.2:c.1174-161_1174-160dup XP_006712863.2:n.1174-161_1174-160dup
XM_011511994.1:c.1060-161_1060-160dup XP_011510296.1:n.1060-161_1060-160dup
XM_011511995.1:c.1165-161_1165-160dup XP_011510297.1:n.1165-161_1165-160dup
XM_011511996.1:c.1015-161_1015-160dup XP_011510298.1:n.1015-161_1015-160dup
XM_011511997.1:c.907-161_907-160dup XP_011510299.1:n.907-161_907-160dup
XM_011511994.3:c.1060-161_1060-160dup XP_011510296.1:n.1060-161_1060-160dup
XM_011511996.2:c.1015-161_1015-160dup XP_011510298.1:n.1015-161_1015-160dup
NM_003590.5:c.1207-161_1207-160dup MANE Select NP_003581.1:n.1207-161_1207-160dup
NM_001257198.2:c.1225-161_1225-160dup NP_001244127.1:n.1225-161_1225-160dup
NM_001257197.2:c.1009-161_1009-160dup NP_001244126.1:n.1009-161_1009-160dup