Canonical Allele Identifier: CA1331555927

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503673T= , CM000664.2:g.224503673T=	GRCh38
NC_000002.11:g.225368390T= , CM000664.1:g.225368390T=	GRCh37
NC_000002.10:g.225076634T=	NCBI36
NG_032169.1:g.86725A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1356A= MANE Select	ENSP00000264414.4:p.Lys452=
ENST00000264414.8:c.1356A=	ENSP00000264414.4:p.Lys452=
ENST00000344951.8:c.1158A=	ENSP00000343601.4:p.Lys386=
ENST00000409096.5:c.1284A=	ENSP00000387200.1:p.Lys428=
ENST00000409777.5:c.1284A=	ENSP00000386525.1:p.Lys428=
ENST00000481135.1:n.652A=
ENST00000617432.4:c.79-1A=	ENSP00000477851.1:n.79-1A=
NM_001257197.1:c.1158A=	NP_001244126.1:p.Lys386=
NM_001257198.1:c.1374A=	NP_001244127.1:p.Lys458=
NM_003590.4:c.1356A=	NP_003581.1:p.Lys452=
XM_006712800.2:c.1323A=	XP_006712863.2:p.Lys441=
XM_011511994.1:c.1209A=	XP_011510296.1:p.Lys403=
XM_011511995.1:c.1314A=	XP_011510297.1:p.Lys438=
XM_011511996.1:c.1164A=	XP_011510298.1:p.Lys388=
XM_011511997.1:c.1056A=	XP_011510299.1:p.Lys352=
XM_011511994.3:c.1209A=	XP_011510296.1:p.Lys403=
XM_011511996.2:c.1164A=	XP_011510298.1:p.Lys388=
NM_003590.5:c.1356A= MANE Select	NP_003581.1:p.Lys452=
NM_001257198.2:c.1374A=	NP_001244127.1:p.Lys458=
NM_001257197.2:c.1158A=	NP_001244126.1:p.Lys386=