Canonical Allele Identifier: CA1331555956

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503791T= , CM000664.2:g.224503791T=	GRCh38
NC_000002.11:g.225368508T= , CM000664.1:g.225368508T=	GRCh37
NC_000002.10:g.225076752T=	NCBI36
NG_032169.1:g.86607A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003590.5:c.1238A= MANE Select	NP_003581.1:p.Asp413=
ENST00000264414.9:c.1238A= MANE Select	ENSP00000264414.4:p.Asp413=
NM_001257197.1:c.1040A=	NP_001244126.1:p.Asp347=
NM_001257197.2:c.1040A=	NP_001244126.1:p.Asp347=
NM_001257198.1:c.1256A=	NP_001244127.1:p.Asp419=
NM_001257198.2:c.1256A=	NP_001244127.1:p.Asp419=
NM_003590.4:c.1238A=	NP_003581.1:p.Asp413=
ENST00000264414.8:c.1238A=	ENSP00000264414.4:p.Asp413=
ENST00000344951.8:c.1040A=	ENSP00000343601.4:p.Asp347=
ENST00000409096.5:c.1166A=	ENSP00000387200.1:p.Asp389=
ENST00000409777.5:c.1166A=	ENSP00000386525.1:p.Asp389=
ENST00000481135.1:n.534A=
ENST00000617432.4:c.-39A=	ENSP00000477851.1:n.-39A=
XM_006712800.2:c.1205A=	XP_006712863.2:p.Asp402=
XM_011511994.1:c.1091A=	XP_011510296.1:p.Asp364=
XM_011511994.3:c.1091A=	XP_011510296.1:p.Asp364=
XM_011511995.1:c.1196A=	XP_011510297.1:p.Asp399=
XM_011511996.1:c.1046A=	XP_011510298.1:p.Asp349=
XM_011511996.2:c.1046A=	XP_011510298.1:p.Asp349=
XM_011511997.1:c.938A=	XP_011510299.1:p.Asp313=