Canonical Allele Identifier: CA1331555949

Gene: CUL3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1263T= MANE Select	ENSP00000264414.4:p.Phe421=
ENST00000264414.8:c.1263T=	ENSP00000264414.4:p.Phe421=
ENST00000344951.8:c.1065T=	ENSP00000343601.4:p.Phe355=
ENST00000409096.5:c.1191T=	ENSP00000387200.1:p.Phe397=
ENST00000409777.5:c.1191T=	ENSP00000386525.1:p.Phe397=
ENST00000481135.1:n.559T=
ENST00000617432.4:c.-14T=	ENSP00000477851.1:n.-14T=
NM_001257197.1:c.1065T=	NP_001244126.1:p.Phe355=
NM_001257198.1:c.1281T=	NP_001244127.1:p.Phe427=
NM_003590.4:c.1263T=	NP_003581.1:p.Phe421=
XM_006712800.2:c.1230T=	XP_006712863.2:p.Phe410=
XM_011511994.1:c.1116T=	XP_011510296.1:p.Phe372=
XM_011511995.1:c.1221T=	XP_011510297.1:p.Phe407=
XM_011511996.1:c.1071T=	XP_011510298.1:p.Phe357=
XM_011511997.1:c.963T=	XP_011510299.1:p.Phe321=
XM_011511994.3:c.1116T=	XP_011510296.1:p.Phe372=
XM_011511996.2:c.1071T=	XP_011510298.1:p.Phe357=
NM_003590.5:c.1263T= MANE Select	NP_003581.1:p.Phe421=
NM_001257198.2:c.1281T=	NP_001244127.1:p.Phe427=
NM_001257197.2:c.1065T=	NP_001244126.1:p.Phe355=