Canonical Allele Identifier: CA350827555

Gene: CUL3

Linked Data

• dbSNP Id: rs749893181
• COSMIC: COSM3743622
• MyVariant Identifiers: chr2:g.225368483A>T (hg19) ; chr2:g.224503766A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503766A>T , CM000664.2:g.224503766A>T	GRCh38
NC_000002.11:g.225368483A>T , CM000664.1:g.225368483A>T	GRCh37
NC_000002.10:g.225076727A>T	NCBI36
NG_032169.1:g.86632T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1263T>A MANE Select	ENSP00000264414.4:p.Phe421Leu
ENST00000264414.8:c.1263T>A	ENSP00000264414.4:p.Phe421Leu
ENST00000344951.8:c.1065T>A	ENSP00000343601.4:p.Phe355Leu
ENST00000409096.5:c.1191T>A	ENSP00000387200.1:p.Phe397Leu
ENST00000409777.5:c.1191T>A	ENSP00000386525.1:p.Phe397Leu
ENST00000481135.1:n.559T>A
ENST00000617432.4:c.-14T>A	ENSP00000477851.1:n.-14T>A
NM_001257197.1:c.1065T>A	NP_001244126.1:p.Phe355Leu
NM_001257198.1:c.1281T>A	NP_001244127.1:p.Phe427Leu
NM_003590.4:c.1263T>A	NP_003581.1:p.Phe421Leu
XM_006712800.2:c.1230T>A	XP_006712863.2:p.Phe410Leu
XM_011511994.1:c.1116T>A	XP_011510296.1:p.Phe372Leu
XM_011511995.1:c.1221T>A	XP_011510297.1:p.Phe407Leu
XM_011511996.1:c.1071T>A	XP_011510298.1:p.Phe357Leu
XM_011511997.1:c.963T>A	XP_011510299.1:p.Phe321Leu
XM_011511994.3:c.1116T>A	XP_011510296.1:p.Phe372Leu
XM_011511996.2:c.1071T>A	XP_011510298.1:p.Phe357Leu
NM_003590.5:c.1263T>A MANE Select	NP_003581.1:p.Phe421Leu
NM_001257198.2:c.1281T>A	NP_001244127.1:p.Phe427Leu
NM_001257197.2:c.1065T>A	NP_001244126.1:p.Phe355Leu