Canonical Allele Identifier: CA765437111

Gene: CUL3

Linked Data

• dbSNP Id: rs1204277950
• gnomAD v3: 2-224504186-T-TA
• gnomAD v4: 2-224504186-T-TA
• MyVariant Identifiers: chr2:g.225368903_225368904insA (hg19) ; chr2:g.224504186_224504187insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224504187dup , CM000664.2:g.224504187dup	GRCh38
NC_000002.11:g.225368904dup , CM000664.1:g.225368904dup	GRCh37
NC_000002.10:g.225077148dup	NCBI36
NG_032169.1:g.86211dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1207-365dup MANE Select	ENSP00000264414.4:n.1207-365dup
ENST00000264414.8:c.1207-365dup	ENSP00000264414.4:n.1207-365dup
ENST00000344951.8:c.1009-365dup	ENSP00000343601.4:n.1009-365dup
ENST00000409096.5:c.1135-365dup	ENSP00000387200.1:n.1135-365dup
ENST00000409777.5:c.1135-365dup	ENSP00000386525.1:n.1135-365dup
ENST00000481135.1:n.138dup
ENST00000617432.4:c.-70-365dup	ENSP00000477851.1:n.-70-365dup
NM_001257197.1:c.1009-365dup	NP_001244126.1:n.1009-365dup
NM_001257198.1:c.1225-365dup	NP_001244127.1:n.1225-365dup
NM_003590.4:c.1207-365dup	NP_003581.1:n.1207-365dup
XM_006712800.2:c.1174-365dup	XP_006712863.2:n.1174-365dup
XM_011511994.1:c.1060-365dup	XP_011510296.1:n.1060-365dup
XM_011511995.1:c.1165-365dup	XP_011510297.1:n.1165-365dup
XM_011511996.1:c.1015-365dup	XP_011510298.1:n.1015-365dup
XM_011511997.1:c.907-365dup	XP_011510299.1:n.907-365dup
XM_011511994.3:c.1060-365dup	XP_011510296.1:n.1060-365dup
XM_011511996.2:c.1015-365dup	XP_011510298.1:n.1015-365dup
NM_003590.5:c.1207-365dup MANE Select	NP_003581.1:n.1207-365dup
NM_001257198.2:c.1225-365dup	NP_001244127.1:n.1225-365dup
NM_001257197.2:c.1009-365dup	NP_001244126.1:n.1009-365dup