Canonical Allele Identifier: CA350827766

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197676
• MyVariant Identifiers: chr2:g.225368533C>G (hg19) ; chr2:g.224503816C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503816C>G , CM000664.2:g.224503816C>G	GRCh38
NC_000002.11:g.225368533C>G , CM000664.1:g.225368533C>G	GRCh37
NC_000002.10:g.225076777C>G	NCBI36
NG_032169.1:g.86582G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1213G>C MANE Select	ENSP00000264414.4:p.Glu405Gln
ENST00000264414.8:c.1213G>C	ENSP00000264414.4:p.Glu405Gln
ENST00000344951.8:c.1015G>C	ENSP00000343601.4:p.Glu339Gln
ENST00000409096.5:c.1141G>C	ENSP00000387200.1:p.Glu381Gln
ENST00000409777.5:c.1141G>C	ENSP00000386525.1:p.Glu381Gln
ENST00000481135.1:n.509G>C
ENST00000617432.4:c.-64G>C	ENSP00000477851.1:n.-64G>C
NM_001257197.1:c.1015G>C	NP_001244126.1:p.Glu339Gln
NM_001257198.1:c.1231G>C	NP_001244127.1:p.Glu411Gln
NM_003590.4:c.1213G>C	NP_003581.1:p.Glu405Gln
XM_006712800.2:c.1180G>C	XP_006712863.2:p.Glu394Gln
XM_011511994.1:c.1066G>C	XP_011510296.1:p.Glu356Gln
XM_011511995.1:c.1171G>C	XP_011510297.1:p.Glu391Gln
XM_011511996.1:c.1021G>C	XP_011510298.1:p.Glu341Gln
XM_011511997.1:c.913G>C	XP_011510299.1:p.Glu305Gln
XM_011511994.3:c.1066G>C	XP_011510296.1:p.Glu356Gln
XM_011511996.2:c.1021G>C	XP_011510298.1:p.Glu341Gln
NM_003590.5:c.1213G>C MANE Select	NP_003581.1:p.Glu405Gln
NM_001257198.2:c.1231G>C	NP_001244127.1:p.Glu411Gln
NM_001257197.2:c.1015G>C	NP_001244126.1:p.Glu339Gln