Canonical Allele Identifier: CA1331555954

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503780C= , CM000664.2:g.224503780C=	GRCh38
NC_000002.11:g.225368497C= , CM000664.1:g.225368497C=	GRCh37
NC_000002.10:g.225076741C=	NCBI36
NG_032169.1:g.86618G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1249G= MANE Select	ENSP00000264414.4:p.Val417=
ENST00000264414.8:c.1249G=	ENSP00000264414.4:p.Val417=
ENST00000344951.8:c.1051G=	ENSP00000343601.4:p.Val351=
ENST00000409096.5:c.1177G=	ENSP00000387200.1:p.Val393=
ENST00000409777.5:c.1177G=	ENSP00000386525.1:p.Val393=
ENST00000481135.1:n.545G=
ENST00000617432.4:c.-28G=	ENSP00000477851.1:n.-28G=
NM_001257197.1:c.1051G=	NP_001244126.1:p.Val351=
NM_001257198.1:c.1267G=	NP_001244127.1:p.Val423=
NM_003590.4:c.1249G=	NP_003581.1:p.Val417=
XM_006712800.2:c.1216G=	XP_006712863.2:p.Val406=
XM_011511994.1:c.1102G=	XP_011510296.1:p.Val368=
XM_011511995.1:c.1207G=	XP_011510297.1:p.Val403=
XM_011511996.1:c.1057G=	XP_011510298.1:p.Val353=
XM_011511997.1:c.949G=	XP_011510299.1:p.Val317=
XM_011511994.3:c.1102G=	XP_011510296.1:p.Val368=
XM_011511996.2:c.1057G=	XP_011510298.1:p.Val353=
NM_003590.5:c.1249G= MANE Select	NP_003581.1:p.Val417=
NM_001257198.2:c.1267G=	NP_001244127.1:p.Val423=
NM_001257197.2:c.1051G=	NP_001244126.1:p.Val351=