Canonical Allele Identifier: CA1331556093

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224504083A= , CM000664.2:g.224504083A=	GRCh38
NC_000002.11:g.225368800A= , CM000664.1:g.225368800A=	GRCh37
NC_000002.10:g.225077044A=	NCBI36
NG_032169.1:g.86315T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1207-261T= MANE Select	ENSP00000264414.4:n.1207-261T=
ENST00000264414.8:c.1207-261T=	ENSP00000264414.4:n.1207-261T=
ENST00000344951.8:c.1009-261T=	ENSP00000343601.4:n.1009-261T=
ENST00000409096.5:c.1135-261T=	ENSP00000387200.1:n.1135-261T=
ENST00000409777.5:c.1135-261T=	ENSP00000386525.1:n.1135-261T=
ENST00000481135.1:n.242T=
ENST00000617432.4:c.-70-261T=	ENSP00000477851.1:n.-70-261T=
NM_001257197.1:c.1009-261T=	NP_001244126.1:n.1009-261T=
NM_001257198.1:c.1225-261T=	NP_001244127.1:n.1225-261T=
NM_003590.4:c.1207-261T=	NP_003581.1:n.1207-261T=
XM_006712800.2:c.1174-261T=	XP_006712863.2:n.1174-261T=
XM_011511994.1:c.1060-261T=	XP_011510296.1:n.1060-261T=
XM_011511995.1:c.1165-261T=	XP_011510297.1:n.1165-261T=
XM_011511996.1:c.1015-261T=	XP_011510298.1:n.1015-261T=
XM_011511997.1:c.907-261T=	XP_011510299.1:n.907-261T=
XM_011511994.3:c.1060-261T=	XP_011510296.1:n.1060-261T=
XM_011511996.2:c.1015-261T=	XP_011510298.1:n.1015-261T=
NM_003590.5:c.1207-261T= MANE Select	NP_003581.1:n.1207-261T=
NM_001257198.2:c.1225-261T=	NP_001244127.1:n.1225-261T=
NM_001257197.2:c.1009-261T=	NP_001244126.1:n.1009-261T=