Canonical Allele Identifier: CA1331555959

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503800G= , CM000664.2:g.224503800G=	GRCh38
NC_000002.11:g.225368517G= , CM000664.1:g.225368517G=	GRCh37
NC_000002.10:g.225076761G=	NCBI36
NG_032169.1:g.86598C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1229C= MANE Select	ENSP00000264414.4:p.Thr410=
ENST00000264414.8:c.1229C=	ENSP00000264414.4:p.Thr410=
ENST00000344951.8:c.1031C=	ENSP00000343601.4:p.Thr344=
ENST00000409096.5:c.1157C=	ENSP00000387200.1:p.Thr386=
ENST00000409777.5:c.1157C=	ENSP00000386525.1:p.Thr386=
ENST00000481135.1:n.525C=
ENST00000617432.4:c.-48C=	ENSP00000477851.1:n.-48C=
NM_001257197.1:c.1031C=	NP_001244126.1:p.Thr344=
NM_001257198.1:c.1247C=	NP_001244127.1:p.Thr416=
NM_003590.4:c.1229C=	NP_003581.1:p.Thr410=
XM_006712800.2:c.1196C=	XP_006712863.2:p.Thr399=
XM_011511994.1:c.1082C=	XP_011510296.1:p.Thr361=
XM_011511995.1:c.1187C=	XP_011510297.1:p.Thr396=
XM_011511996.1:c.1037C=	XP_011510298.1:p.Thr346=
XM_011511997.1:c.929C=	XP_011510299.1:p.Thr310=
XM_011511994.3:c.1082C=	XP_011510296.1:p.Thr361=
XM_011511996.2:c.1037C=	XP_011510298.1:p.Thr346=
NM_003590.5:c.1229C= MANE Select	NP_003581.1:p.Thr410=
NM_001257198.2:c.1247C=	NP_001244127.1:p.Thr416=
NM_001257197.2:c.1031C=	NP_001244126.1:p.Thr344=