Canonical Allele Identifier: CA1331555932

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503691A= , CM000664.2:g.224503691A=	GRCh38
NC_000002.11:g.225368408A= , CM000664.1:g.225368408A=	GRCh37
NC_000002.10:g.225076652A=	NCBI36
NG_032169.1:g.86707T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1338T= MANE Select	ENSP00000264414.4:p.Val446=
ENST00000264414.8:c.1338T=	ENSP00000264414.4:p.Val446=
ENST00000344951.8:c.1140T=	ENSP00000343601.4:p.Val380=
ENST00000409096.5:c.1266T=	ENSP00000387200.1:p.Val422=
ENST00000409777.5:c.1266T=	ENSP00000386525.1:p.Val422=
ENST00000481135.1:n.634T=
ENST00000617432.4:c.62T=	ENSP00000477851.1:p.Phe21=
NM_001257197.1:c.1140T=	NP_001244126.1:p.Val380=
NM_001257198.1:c.1356T=	NP_001244127.1:p.Val452=
NM_003590.4:c.1338T=	NP_003581.1:p.Val446=
XM_006712800.2:c.1305T=	XP_006712863.2:p.Val435=
XM_011511994.1:c.1191T=	XP_011510296.1:p.Val397=
XM_011511995.1:c.1296T=	XP_011510297.1:p.Val432=
XM_011511996.1:c.1146T=	XP_011510298.1:p.Val382=
XM_011511997.1:c.1038T=	XP_011510299.1:p.Val346=
XM_011511994.3:c.1191T=	XP_011510296.1:p.Val397=
XM_011511996.2:c.1146T=	XP_011510298.1:p.Val382=
NM_003590.5:c.1338T= MANE Select	NP_003581.1:p.Val446=
NM_001257198.2:c.1356T=	NP_001244127.1:p.Val452=
NM_001257197.2:c.1140T=	NP_001244126.1:p.Val380=