Canonical Allele Identifier: CA1331555953

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503777G= , CM000664.2:g.224503777G=	GRCh38
NC_000002.11:g.225368494G= , CM000664.1:g.225368494G=	GRCh37
NC_000002.10:g.225076738G=	NCBI36
NG_032169.1:g.86621C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1252C= MANE Select	ENSP00000264414.4:p.Leu418=
ENST00000264414.8:c.1252C=	ENSP00000264414.4:p.Leu418=
ENST00000344951.8:c.1054C=	ENSP00000343601.4:p.Leu352=
ENST00000409096.5:c.1180C=	ENSP00000387200.1:p.Leu394=
ENST00000409777.5:c.1180C=	ENSP00000386525.1:p.Leu394=
ENST00000481135.1:n.548C=
ENST00000617432.4:c.-25C=	ENSP00000477851.1:n.-25C=
NM_001257197.1:c.1054C=	NP_001244126.1:p.Leu352=
NM_001257198.1:c.1270C=	NP_001244127.1:p.Leu424=
NM_003590.4:c.1252C=	NP_003581.1:p.Leu418=
XM_006712800.2:c.1219C=	XP_006712863.2:p.Leu407=
XM_011511994.1:c.1105C=	XP_011510296.1:p.Leu369=
XM_011511995.1:c.1210C=	XP_011510297.1:p.Leu404=
XM_011511996.1:c.1060C=	XP_011510298.1:p.Leu354=
XM_011511997.1:c.952C=	XP_011510299.1:p.Leu318=
XM_011511994.3:c.1105C=	XP_011510296.1:p.Leu369=
XM_011511996.2:c.1060C=	XP_011510298.1:p.Leu354=
NM_003590.5:c.1252C= MANE Select	NP_003581.1:p.Leu418=
NM_001257198.2:c.1270C=	NP_001244127.1:p.Leu424=
NM_001257197.2:c.1054C=	NP_001244126.1:p.Leu352=