Canonical Allele Identifier: CA1331555937

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503703T= , CM000664.2:g.224503703T=	GRCh38
NC_000002.11:g.225368420T= , CM000664.1:g.225368420T=	GRCh37
NC_000002.10:g.225076664T=	NCBI36
NG_032169.1:g.86695A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1326A= MANE Select	ENSP00000264414.4:p.Thr442=
ENST00000264414.8:c.1326A=	ENSP00000264414.4:p.Thr442=
ENST00000344951.8:c.1128A=	ENSP00000343601.4:p.Thr376=
ENST00000409096.5:c.1254A=	ENSP00000387200.1:p.Thr418=
ENST00000409777.5:c.1254A=	ENSP00000386525.1:p.Thr418=
ENST00000481135.1:n.622A=
ENST00000617432.4:c.50A=	ENSP00000477851.1:p.Gln17=
NM_001257197.1:c.1128A=	NP_001244126.1:p.Thr376=
NM_001257198.1:c.1344A=	NP_001244127.1:p.Thr448=
NM_003590.4:c.1326A=	NP_003581.1:p.Thr442=
XM_006712800.2:c.1293A=	XP_006712863.2:p.Thr431=
XM_011511994.1:c.1179A=	XP_011510296.1:p.Thr393=
XM_011511995.1:c.1284A=	XP_011510297.1:p.Thr428=
XM_011511996.1:c.1134A=	XP_011510298.1:p.Thr378=
XM_011511997.1:c.1026A=	XP_011510299.1:p.Thr342=
XM_011511994.3:c.1179A=	XP_011510296.1:p.Thr393=
XM_011511996.2:c.1134A=	XP_011510298.1:p.Thr378=
NM_003590.5:c.1326A= MANE Select	NP_003581.1:p.Thr442=
NM_001257198.2:c.1344A=	NP_001244127.1:p.Thr448=
NM_001257197.2:c.1128A=	NP_001244126.1:p.Thr376=