Canonical Allele Identifier: CA350827536

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197222
• MyVariant Identifiers: chr2:g.225368476C>G (hg19) ; chr2:g.224503759C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503759C>G , CM000664.2:g.224503759C>G	GRCh38
NC_000002.11:g.225368476C>G , CM000664.1:g.225368476C>G	GRCh37
NC_000002.10:g.225076720C>G	NCBI36
NG_032169.1:g.86639G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1270G>C MANE Select	ENSP00000264414.4:p.Glu424Gln
ENST00000264414.8:c.1270G>C	ENSP00000264414.4:p.Glu424Gln
ENST00000344951.8:c.1072G>C	ENSP00000343601.4:p.Glu358Gln
ENST00000409096.5:c.1198G>C	ENSP00000387200.1:p.Glu400Gln
ENST00000409777.5:c.1198G>C	ENSP00000386525.1:p.Glu400Gln
ENST00000481135.1:n.566G>C
ENST00000617432.4:c.-7G>C	ENSP00000477851.1:n.-7G>C
NM_001257197.1:c.1072G>C	NP_001244126.1:p.Glu358Gln
NM_001257198.1:c.1288G>C	NP_001244127.1:p.Glu430Gln
NM_003590.4:c.1270G>C	NP_003581.1:p.Glu424Gln
XM_006712800.2:c.1237G>C	XP_006712863.2:p.Glu413Gln
XM_011511994.1:c.1123G>C	XP_011510296.1:p.Glu375Gln
XM_011511995.1:c.1228G>C	XP_011510297.1:p.Glu410Gln
XM_011511996.1:c.1078G>C	XP_011510298.1:p.Glu360Gln
XM_011511997.1:c.970G>C	XP_011510299.1:p.Glu324Gln
XM_011511994.3:c.1123G>C	XP_011510296.1:p.Glu375Gln
XM_011511996.2:c.1078G>C	XP_011510298.1:p.Glu360Gln
NM_003590.5:c.1270G>C MANE Select	NP_003581.1:p.Glu424Gln
NM_001257198.2:c.1288G>C	NP_001244127.1:p.Glu430Gln
NM_001257197.2:c.1072G>C	NP_001244126.1:p.Glu358Gln