Canonical Allele Identifier: CA2663372687

Gene: CUL3

Linked Data

• gnomAD v4: 2-224504117-G-GGGCCGGGCGCGGTGGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224504117_224504118insGGCCGGGCGCGGTGGCT , CM000664.2:g.224504117_224504118insGGCCGGGCGCGGTGGCT	GRCh38
NC_000002.11:g.225368834_225368835insGGCCGGGCGCGGTGGCT , CM000664.1:g.225368834_225368835insGGCCGGGCGCGGTGGCT	GRCh37
NC_000002.10:g.225077078_225077079insGGCCGGGCGCGGTGGCT	NCBI36
NG_032169.1:g.86280_86281insAGCCACCGCGCCCGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1207-296_1207-295insAGCCACCGCGCCCGGCC MANE Select	ENSP00000264414.4:n.1207-296_1207-295insAGCCACCGCGCCCGGCC
ENST00000264414.8:c.1207-296_1207-295insAGCCACCGCGCCCGGCC	ENSP00000264414.4:n.1207-296_1207-295insAGCCACCGCGCCCGGCC
ENST00000344951.8:c.1009-296_1009-295insAGCCACCGCGCCCGGCC	ENSP00000343601.4:n.1009-296_1009-295insAGCCACCGCGCCCGGCC
ENST00000409096.5:c.1135-296_1135-295insAGCCACCGCGCCCGGCC	ENSP00000387200.1:n.1135-296_1135-295insAGCCACCGCGCCCGGCC
ENST00000409777.5:c.1135-296_1135-295insAGCCACCGCGCCCGGCC	ENSP00000386525.1:n.1135-296_1135-295insAGCCACCGCGCCCGGCC
ENST00000481135.1:n.207_208insAGCCACCGCGCCCGGCC
ENST00000617432.4:c.-70-296_-70-295insAGCCACCGCGCCCGGCC	ENSP00000477851.1:n.-70-296_-70-295insAGCCACCGCGCCCGGCC
NM_001257197.1:c.1009-296_1009-295insAGCCACCGCGCCCGGCC	NP_001244126.1:n.1009-296_1009-295insAGCCACCGCGCCCGGCC
NM_001257198.1:c.1225-296_1225-295insAGCCACCGCGCCCGGCC	NP_001244127.1:n.1225-296_1225-295insAGCCACCGCGCCCGGCC
NM_003590.4:c.1207-296_1207-295insAGCCACCGCGCCCGGCC	NP_003581.1:n.1207-296_1207-295insAGCCACCGCGCCCGGCC
XM_006712800.2:c.1174-296_1174-295insAGCCACCGCGCCCGGCC	XP_006712863.2:n.1174-296_1174-295insAGCCACCGCGCCCGGCC
XM_011511994.1:c.1060-296_1060-295insAGCCACCGCGCCCGGCC	XP_011510296.1:n.1060-296_1060-295insAGCCACCGCGCCCGGCC
XM_011511995.1:c.1165-296_1165-295insAGCCACCGCGCCCGGCC	XP_011510297.1:n.1165-296_1165-295insAGCCACCGCGCCCGGCC
XM_011511996.1:c.1015-296_1015-295insAGCCACCGCGCCCGGCC	XP_011510298.1:n.1015-296_1015-295insAGCCACCGCGCCCGGCC
XM_011511997.1:c.907-296_907-295insAGCCACCGCGCCCGGCC	XP_011510299.1:n.907-296_907-295insAGCCACCGCGCCCGGCC
XM_011511994.3:c.1060-296_1060-295insAGCCACCGCGCCCGGCC	XP_011510296.1:n.1060-296_1060-295insAGCCACCGCGCCCGGCC
XM_011511996.2:c.1015-296_1015-295insAGCCACCGCGCCCGGCC	XP_011510298.1:n.1015-296_1015-295insAGCCACCGCGCCCGGCC
NM_003590.5:c.1207-296_1207-295insAGCCACCGCGCCCGGCC MANE Select	NP_003581.1:n.1207-296_1207-295insAGCCACCGCGCCCGGCC
NM_001257198.2:c.1225-296_1225-295insAGCCACCGCGCCCGGCC	NP_001244127.1:n.1225-296_1225-295insAGCCACCGCGCCCGGCC
NM_001257197.2:c.1009-296_1009-295insAGCCACCGCGCCCGGCC	NP_001244126.1:n.1009-296_1009-295insAGCCACCGCGCCCGGCC