Canonical Allele Identifier: CA1331555931

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503688A= , CM000664.2:g.224503688A=	GRCh38
NC_000002.11:g.225368405A= , CM000664.1:g.225368405A=	GRCh37
NC_000002.10:g.225076649A=	NCBI36
NG_032169.1:g.86710T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1341T= MANE Select	ENSP00000264414.4:p.Ser447=
ENST00000264414.8:c.1341T=	ENSP00000264414.4:p.Ser447=
ENST00000344951.8:c.1143T=	ENSP00000343601.4:p.Ser381=
ENST00000409096.5:c.1269T=	ENSP00000387200.1:p.Ser423=
ENST00000409777.5:c.1269T=	ENSP00000386525.1:p.Ser423=
ENST00000481135.1:n.637T=
ENST00000617432.4:c.65T=	ENSP00000477851.1:p.Leu22=
NM_001257197.1:c.1143T=	NP_001244126.1:p.Ser381=
NM_001257198.1:c.1359T=	NP_001244127.1:p.Ser453=
NM_003590.4:c.1341T=	NP_003581.1:p.Ser447=
XM_006712800.2:c.1308T=	XP_006712863.2:p.Ser436=
XM_011511994.1:c.1194T=	XP_011510296.1:p.Ser398=
XM_011511995.1:c.1299T=	XP_011510297.1:p.Ser433=
XM_011511996.1:c.1149T=	XP_011510298.1:p.Ser383=
XM_011511997.1:c.1041T=	XP_011510299.1:p.Ser347=
XM_011511994.3:c.1194T=	XP_011510296.1:p.Ser398=
XM_011511996.2:c.1149T=	XP_011510298.1:p.Ser383=
NM_003590.5:c.1341T= MANE Select	NP_003581.1:p.Ser447=
NM_001257198.2:c.1359T=	NP_001244127.1:p.Ser453=
NM_001257197.2:c.1143T=	NP_001244126.1:p.Ser381=