Canonical Allele Identifier: CA350827557

Gene: CUL3

Linked Data

• dbSNP Id: rs1692487093
• MyVariant Identifiers: chr2:g.225368484A>T (hg19) ; chr2:g.224503767A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503767A>T , CM000664.2:g.224503767A>T	GRCh38
NC_000002.11:g.225368484A>T , CM000664.1:g.225368484A>T	GRCh37
NC_000002.10:g.225076728A>T	NCBI36
NG_032169.1:g.86631T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1262T>A MANE Select	ENSP00000264414.4:p.Phe421Tyr
ENST00000264414.8:c.1262T>A	ENSP00000264414.4:p.Phe421Tyr
ENST00000344951.8:c.1064T>A	ENSP00000343601.4:p.Phe355Tyr
ENST00000409096.5:c.1190T>A	ENSP00000387200.1:p.Phe397Tyr
ENST00000409777.5:c.1190T>A	ENSP00000386525.1:p.Phe397Tyr
ENST00000481135.1:n.558T>A
ENST00000617432.4:c.-15T>A	ENSP00000477851.1:n.-15T>A
NM_001257197.1:c.1064T>A	NP_001244126.1:p.Phe355Tyr
NM_001257198.1:c.1280T>A	NP_001244127.1:p.Phe427Tyr
NM_003590.4:c.1262T>A	NP_003581.1:p.Phe421Tyr
XM_006712800.2:c.1229T>A	XP_006712863.2:p.Phe410Tyr
XM_011511994.1:c.1115T>A	XP_011510296.1:p.Phe372Tyr
XM_011511995.1:c.1220T>A	XP_011510297.1:p.Phe407Tyr
XM_011511996.1:c.1070T>A	XP_011510298.1:p.Phe357Tyr
XM_011511997.1:c.962T>A	XP_011510299.1:p.Phe321Tyr
XM_011511994.3:c.1115T>A	XP_011510296.1:p.Phe372Tyr
XM_011511996.2:c.1070T>A	XP_011510298.1:p.Phe357Tyr
NM_003590.5:c.1262T>A MANE Select	NP_003581.1:p.Phe421Tyr
NM_001257198.2:c.1280T>A	NP_001244127.1:p.Phe427Tyr
NM_001257197.2:c.1064T>A	NP_001244126.1:p.Phe355Tyr