Canonical Allele Identifier: CA350827711

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197572
• MyVariant Identifiers: chr2:g.225368520T>A (hg19) ; chr2:g.224503803T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503803T>A , CM000664.2:g.224503803T>A	GRCh38
NC_000002.11:g.225368520T>A , CM000664.1:g.225368520T>A	GRCh37
NC_000002.10:g.225076764T>A	NCBI36
NG_032169.1:g.86595A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1226A>T MANE Select	ENSP00000264414.4:p.Glu409Val
ENST00000264414.8:c.1226A>T	ENSP00000264414.4:p.Glu409Val
ENST00000344951.8:c.1028A>T	ENSP00000343601.4:p.Glu343Val
ENST00000409096.5:c.1154A>T	ENSP00000387200.1:p.Glu385Val
ENST00000409777.5:c.1154A>T	ENSP00000386525.1:p.Glu385Val
ENST00000481135.1:n.522A>T
ENST00000617432.4:c.-51A>T	ENSP00000477851.1:n.-51A>T
NM_001257197.1:c.1028A>T	NP_001244126.1:p.Glu343Val
NM_001257198.1:c.1244A>T	NP_001244127.1:p.Glu415Val
NM_003590.4:c.1226A>T	NP_003581.1:p.Glu409Val
XM_006712800.2:c.1193A>T	XP_006712863.2:p.Glu398Val
XM_011511994.1:c.1079A>T	XP_011510296.1:p.Glu360Val
XM_011511995.1:c.1184A>T	XP_011510297.1:p.Glu395Val
XM_011511996.1:c.1034A>T	XP_011510298.1:p.Glu345Val
XM_011511997.1:c.926A>T	XP_011510299.1:p.Glu309Val
XM_011511994.3:c.1079A>T	XP_011510296.1:p.Glu360Val
XM_011511996.2:c.1034A>T	XP_011510298.1:p.Glu345Val
NM_003590.5:c.1226A>T MANE Select	NP_003581.1:p.Glu409Val
NM_001257198.2:c.1244A>T	NP_001244127.1:p.Glu415Val
NM_001257197.2:c.1028A>T	NP_001244126.1:p.Glu343Val