Canonical Allele Identifier: CA1331555925

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503669T= , CM000664.2:g.224503669T=	GRCh38
NC_000002.11:g.225368386T= , CM000664.1:g.225368386T=	GRCh37
NC_000002.10:g.225076630T=	NCBI36
NG_032169.1:g.86729A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1360A= MANE Select	ENSP00000264414.4:p.Met454=
ENST00000264414.8:c.1360A=	ENSP00000264414.4:p.Met454=
ENST00000344951.8:c.1162A=	ENSP00000343601.4:p.Met388=
ENST00000409096.5:c.1288A=	ENSP00000387200.1:p.Met430=
ENST00000409777.5:c.1288A=	ENSP00000386525.1:p.Met430=
ENST00000481135.1:n.656A=
ENST00000617432.4:c.82A=	ENSP00000477851.1:p.Met28=
NM_001257197.1:c.1162A=	NP_001244126.1:p.Met388=
NM_001257198.1:c.1378A=	NP_001244127.1:p.Met460=
NM_003590.4:c.1360A=	NP_003581.1:p.Met454=
XM_006712800.2:c.1327A=	XP_006712863.2:p.Met443=
XM_011511994.1:c.1213A=	XP_011510296.1:p.Met405=
XM_011511995.1:c.1318A=	XP_011510297.1:p.Met440=
XM_011511996.1:c.1168A=	XP_011510298.1:p.Met390=
XM_011511997.1:c.1060A=	XP_011510299.1:p.Met354=
XM_011511994.3:c.1213A=	XP_011510296.1:p.Met405=
XM_011511996.2:c.1168A=	XP_011510298.1:p.Met390=
NM_003590.5:c.1360A= MANE Select	NP_003581.1:p.Met454=
NM_001257198.2:c.1378A=	NP_001244127.1:p.Met460=
NM_001257197.2:c.1162A=	NP_001244126.1:p.Met388=