Canonical Allele Identifier: CA350827545

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197241
• MyVariant Identifiers: chr2:g.225368479G>C (hg19) ; chr2:g.224503762G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503762G>C , CM000664.2:g.224503762G>C	GRCh38
NC_000002.11:g.225368479G>C , CM000664.1:g.225368479G>C	GRCh37
NC_000002.10:g.225076723G>C	NCBI36
NG_032169.1:g.86636C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1267C>G MANE Select	ENSP00000264414.4:p.Gln423Glu
ENST00000264414.8:c.1267C>G	ENSP00000264414.4:p.Gln423Glu
ENST00000344951.8:c.1069C>G	ENSP00000343601.4:p.Gln357Glu
ENST00000409096.5:c.1195C>G	ENSP00000387200.1:p.Gln399Glu
ENST00000409777.5:c.1195C>G	ENSP00000386525.1:p.Gln399Glu
ENST00000481135.1:n.563C>G
ENST00000617432.4:c.-10C>G	ENSP00000477851.1:n.-10C>G
NM_001257197.1:c.1069C>G	NP_001244126.1:p.Gln357Glu
NM_001257198.1:c.1285C>G	NP_001244127.1:p.Gln429Glu
NM_003590.4:c.1267C>G	NP_003581.1:p.Gln423Glu
XM_006712800.2:c.1234C>G	XP_006712863.2:p.Gln412Glu
XM_011511994.1:c.1120C>G	XP_011510296.1:p.Gln374Glu
XM_011511995.1:c.1225C>G	XP_011510297.1:p.Gln409Glu
XM_011511996.1:c.1075C>G	XP_011510298.1:p.Gln359Glu
XM_011511997.1:c.967C>G	XP_011510299.1:p.Gln323Glu
XM_011511994.3:c.1120C>G	XP_011510296.1:p.Gln374Glu
XM_011511996.2:c.1075C>G	XP_011510298.1:p.Gln359Glu
NM_003590.5:c.1267C>G MANE Select	NP_003581.1:p.Gln423Glu
NM_001257198.2:c.1285C>G	NP_001244127.1:p.Gln429Glu
NM_001257197.2:c.1069C>G	NP_001244126.1:p.Gln357Glu