Canonical Allele Identifier: CA1331555958

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503799T= , CM000664.2:g.224503799T=	GRCh38
NC_000002.11:g.225368516T= , CM000664.1:g.225368516T=	GRCh37
NC_000002.10:g.225076760T=	NCBI36
NG_032169.1:g.86599A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1230A= MANE Select	ENSP00000264414.4:p.Thr410=
ENST00000264414.8:c.1230A=	ENSP00000264414.4:p.Thr410=
ENST00000344951.8:c.1032A=	ENSP00000343601.4:p.Thr344=
ENST00000409096.5:c.1158A=	ENSP00000387200.1:p.Thr386=
ENST00000409777.5:c.1158A=	ENSP00000386525.1:p.Thr386=
ENST00000481135.1:n.526A=
ENST00000617432.4:c.-47A=	ENSP00000477851.1:n.-47A=
NM_001257197.1:c.1032A=	NP_001244126.1:p.Thr344=
NM_001257198.1:c.1248A=	NP_001244127.1:p.Thr416=
NM_003590.4:c.1230A=	NP_003581.1:p.Thr410=
XM_006712800.2:c.1197A=	XP_006712863.2:p.Thr399=
XM_011511994.1:c.1083A=	XP_011510296.1:p.Thr361=
XM_011511995.1:c.1188A=	XP_011510297.1:p.Thr396=
XM_011511996.1:c.1038A=	XP_011510298.1:p.Thr346=
XM_011511997.1:c.930A=	XP_011510299.1:p.Thr310=
XM_011511994.3:c.1083A=	XP_011510296.1:p.Thr361=
XM_011511996.2:c.1038A=	XP_011510298.1:p.Thr346=
NM_003590.5:c.1230A= MANE Select	NP_003581.1:p.Thr410=
NM_001257198.2:c.1248A=	NP_001244127.1:p.Thr416=
NM_001257197.2:c.1032A=	NP_001244126.1:p.Thr344=