Canonical Allele Identifier: CA350827573

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197314
• MyVariant Identifiers: chr2:g.225368487C>T (hg19) ; chr2:g.224503770C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503770C>T , CM000664.2:g.224503770C>T	GRCh38
NC_000002.11:g.225368487C>T , CM000664.1:g.225368487C>T	GRCh37
NC_000002.10:g.225076731C>T	NCBI36
NG_032169.1:g.86628G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1259G>A MANE Select	ENSP00000264414.4:p.Arg420Lys
ENST00000264414.8:c.1259G>A	ENSP00000264414.4:p.Arg420Lys
ENST00000344951.8:c.1061G>A	ENSP00000343601.4:p.Arg354Lys
ENST00000409096.5:c.1187G>A	ENSP00000387200.1:p.Arg396Lys
ENST00000409777.5:c.1187G>A	ENSP00000386525.1:p.Arg396Lys
ENST00000481135.1:n.555G>A
ENST00000617432.4:c.-18G>A	ENSP00000477851.1:n.-18G>A
NM_001257197.1:c.1061G>A	NP_001244126.1:p.Arg354Lys
NM_001257198.1:c.1277G>A	NP_001244127.1:p.Arg426Lys
NM_003590.4:c.1259G>A	NP_003581.1:p.Arg420Lys
XM_006712800.2:c.1226G>A	XP_006712863.2:p.Arg409Lys
XM_011511994.1:c.1112G>A	XP_011510296.1:p.Arg371Lys
XM_011511995.1:c.1217G>A	XP_011510297.1:p.Arg406Lys
XM_011511996.1:c.1067G>A	XP_011510298.1:p.Arg356Lys
XM_011511997.1:c.959G>A	XP_011510299.1:p.Arg320Lys
XM_011511994.3:c.1112G>A	XP_011510296.1:p.Arg371Lys
XM_011511996.2:c.1067G>A	XP_011510298.1:p.Arg356Lys
NM_003590.5:c.1259G>A MANE Select	NP_003581.1:p.Arg420Lys
NM_001257198.2:c.1277G>A	NP_001244127.1:p.Arg426Lys
NM_001257197.2:c.1061G>A	NP_001244126.1:p.Arg354Lys