Canonical Allele Identifier: CA1331555933

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503694A= , CM000664.2:g.224503694A=	GRCh38
NC_000002.11:g.225368411A= , CM000664.1:g.225368411A=	GRCh37
NC_000002.10:g.225076655A=	NCBI36
NG_032169.1:g.86704T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1335T= MANE Select	ENSP00000264414.4:p.Ser445=
ENST00000264414.8:c.1335T=	ENSP00000264414.4:p.Ser445=
ENST00000344951.8:c.1137T=	ENSP00000343601.4:p.Ser379=
ENST00000409096.5:c.1263T=	ENSP00000387200.1:p.Ser421=
ENST00000409777.5:c.1263T=	ENSP00000386525.1:p.Ser421=
ENST00000481135.1:n.631T=
ENST00000617432.4:c.59T=	ENSP00000477851.1:p.Val20=
NM_001257197.1:c.1137T=	NP_001244126.1:p.Ser379=
NM_001257198.1:c.1353T=	NP_001244127.1:p.Ser451=
NM_003590.4:c.1335T=	NP_003581.1:p.Ser445=
XM_006712800.2:c.1302T=	XP_006712863.2:p.Ser434=
XM_011511994.1:c.1188T=	XP_011510296.1:p.Ser396=
XM_011511995.1:c.1293T=	XP_011510297.1:p.Ser431=
XM_011511996.1:c.1143T=	XP_011510298.1:p.Ser381=
XM_011511997.1:c.1035T=	XP_011510299.1:p.Ser345=
XM_011511994.3:c.1188T=	XP_011510296.1:p.Ser396=
XM_011511996.2:c.1143T=	XP_011510298.1:p.Ser381=
NM_003590.5:c.1335T= MANE Select	NP_003581.1:p.Ser445=
NM_001257198.2:c.1353T=	NP_001244127.1:p.Ser451=
NM_001257197.2:c.1137T=	NP_001244126.1:p.Ser379=