Canonical Allele Identifier: CA350827532

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197213
• MyVariant Identifiers: chr2:g.225368475T>A (hg19) ; chr2:g.224503758T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503758T>A , CM000664.2:g.224503758T>A	GRCh38
NC_000002.11:g.225368475T>A , CM000664.1:g.225368475T>A	GRCh37
NC_000002.10:g.225076719T>A	NCBI36
NG_032169.1:g.86640A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1271A>T MANE Select	ENSP00000264414.4:p.Glu424Val
ENST00000264414.8:c.1271A>T	ENSP00000264414.4:p.Glu424Val
ENST00000344951.8:c.1073A>T	ENSP00000343601.4:p.Glu358Val
ENST00000409096.5:c.1199A>T	ENSP00000387200.1:p.Glu400Val
ENST00000409777.5:c.1199A>T	ENSP00000386525.1:p.Glu400Val
ENST00000481135.1:n.567A>T
ENST00000617432.4:c.-6A>T	ENSP00000477851.1:n.-6A>T
NM_001257197.1:c.1073A>T	NP_001244126.1:p.Glu358Val
NM_001257198.1:c.1289A>T	NP_001244127.1:p.Glu430Val
NM_003590.4:c.1271A>T	NP_003581.1:p.Glu424Val
XM_006712800.2:c.1238A>T	XP_006712863.2:p.Glu413Val
XM_011511994.1:c.1124A>T	XP_011510296.1:p.Glu375Val
XM_011511995.1:c.1229A>T	XP_011510297.1:p.Glu410Val
XM_011511996.1:c.1079A>T	XP_011510298.1:p.Glu360Val
XM_011511997.1:c.971A>T	XP_011510299.1:p.Glu324Val
XM_011511994.3:c.1124A>T	XP_011510296.1:p.Glu375Val
XM_011511996.2:c.1079A>T	XP_011510298.1:p.Glu360Val
NM_003590.5:c.1271A>T MANE Select	NP_003581.1:p.Glu424Val
NM_001257198.2:c.1289A>T	NP_001244127.1:p.Glu430Val
NM_001257197.2:c.1073A>T	NP_001244126.1:p.Glu358Val