Canonical Allele Identifier: CA350827279

Gene: CUL3

Linked Data

• dbSNP Id: rs757797000
• MyVariant Identifiers: chr2:g.225368429T>A (hg19) ; chr2:g.224503712T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503712T>A , CM000664.2:g.224503712T>A	GRCh38
NC_000002.11:g.225368429T>A , CM000664.1:g.225368429T>A	GRCh37
NC_000002.10:g.225076673T>A	NCBI36
NG_032169.1:g.86686A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1317A>T MANE Select	ENSP00000264414.4:p.Arg439Ser
ENST00000264414.8:c.1317A>T	ENSP00000264414.4:p.Arg439Ser
ENST00000344951.8:c.1119A>T	ENSP00000343601.4:p.Arg373Ser
ENST00000409096.5:c.1245A>T	ENSP00000387200.1:p.Arg415Ser
ENST00000409777.5:c.1245A>T	ENSP00000386525.1:p.Arg415Ser
ENST00000481135.1:n.613A>T
ENST00000617432.4:c.41A>T	ENSP00000477851.1:p.Asp14Val
NM_001257197.1:c.1119A>T	NP_001244126.1:p.Arg373Ser
NM_001257198.1:c.1335A>T	NP_001244127.1:p.Arg445Ser
NM_003590.4:c.1317A>T	NP_003581.1:p.Arg439Ser
XM_006712800.2:c.1284A>T	XP_006712863.2:p.Arg428Ser
XM_011511994.1:c.1170A>T	XP_011510296.1:p.Arg390Ser
XM_011511995.1:c.1275A>T	XP_011510297.1:p.Arg425Ser
XM_011511996.1:c.1125A>T	XP_011510298.1:p.Arg375Ser
XM_011511997.1:c.1017A>T	XP_011510299.1:p.Arg339Ser
XM_011511994.3:c.1170A>T	XP_011510296.1:p.Arg390Ser
XM_011511996.2:c.1125A>T	XP_011510298.1:p.Arg375Ser
NM_003590.5:c.1317A>T MANE Select	NP_003581.1:p.Arg439Ser
NM_001257198.2:c.1335A>T	NP_001244127.1:p.Arg445Ser
NM_001257197.2:c.1119A>T	NP_001244126.1:p.Arg373Ser