Canonical Allele Identifier: CA1331555951

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503772A= , CM000664.2:g.224503772A=	GRCh38
NC_000002.11:g.225368489A= , CM000664.1:g.225368489A=	GRCh37
NC_000002.10:g.225076733A=	NCBI36
NG_032169.1:g.86626T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1257T= MANE Select	ENSP00000264414.4:p.Phe419=
ENST00000264414.8:c.1257T=	ENSP00000264414.4:p.Phe419=
ENST00000344951.8:c.1059T=	ENSP00000343601.4:p.Phe353=
ENST00000409096.5:c.1185T=	ENSP00000387200.1:p.Phe395=
ENST00000409777.5:c.1185T=	ENSP00000386525.1:p.Phe395=
ENST00000481135.1:n.553T=
ENST00000617432.4:c.-20T=	ENSP00000477851.1:n.-20T=
NM_001257197.1:c.1059T=	NP_001244126.1:p.Phe353=
NM_001257198.1:c.1275T=	NP_001244127.1:p.Phe425=
NM_003590.4:c.1257T=	NP_003581.1:p.Phe419=
XM_006712800.2:c.1224T=	XP_006712863.2:p.Phe408=
XM_011511994.1:c.1110T=	XP_011510296.1:p.Phe370=
XM_011511995.1:c.1215T=	XP_011510297.1:p.Phe405=
XM_011511996.1:c.1065T=	XP_011510298.1:p.Phe355=
XM_011511997.1:c.957T=	XP_011510299.1:p.Phe319=
XM_011511994.3:c.1110T=	XP_011510296.1:p.Phe370=
XM_011511996.2:c.1065T=	XP_011510298.1:p.Phe355=
NM_003590.5:c.1257T= MANE Select	NP_003581.1:p.Phe419=
NM_001257198.2:c.1275T=	NP_001244127.1:p.Phe425=
NM_001257197.2:c.1059T=	NP_001244126.1:p.Phe353=