Canonical Allele Identifier: CA350827567

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197304
• MyVariant Identifiers: chr2:g.225368486C>G (hg19) ; chr2:g.224503769C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503769C>G , CM000664.2:g.224503769C>G	GRCh38
NC_000002.11:g.225368486C>G , CM000664.1:g.225368486C>G	GRCh37
NC_000002.10:g.225076730C>G	NCBI36
NG_032169.1:g.86629G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1260G>C MANE Select	ENSP00000264414.4:p.Arg420Ser
ENST00000264414.8:c.1260G>C	ENSP00000264414.4:p.Arg420Ser
ENST00000344951.8:c.1062G>C	ENSP00000343601.4:p.Arg354Ser
ENST00000409096.5:c.1188G>C	ENSP00000387200.1:p.Arg396Ser
ENST00000409777.5:c.1188G>C	ENSP00000386525.1:p.Arg396Ser
ENST00000481135.1:n.556G>C
ENST00000617432.4:c.-17G>C	ENSP00000477851.1:n.-17G>C
NM_001257197.1:c.1062G>C	NP_001244126.1:p.Arg354Ser
NM_001257198.1:c.1278G>C	NP_001244127.1:p.Arg426Ser
NM_003590.4:c.1260G>C	NP_003581.1:p.Arg420Ser
XM_006712800.2:c.1227G>C	XP_006712863.2:p.Arg409Ser
XM_011511994.1:c.1113G>C	XP_011510296.1:p.Arg371Ser
XM_011511995.1:c.1218G>C	XP_011510297.1:p.Arg406Ser
XM_011511996.1:c.1068G>C	XP_011510298.1:p.Arg356Ser
XM_011511997.1:c.960G>C	XP_011510299.1:p.Arg320Ser
XM_011511994.3:c.1113G>C	XP_011510296.1:p.Arg371Ser
XM_011511996.2:c.1068G>C	XP_011510298.1:p.Arg356Ser
NM_003590.5:c.1260G>C MANE Select	NP_003581.1:p.Arg420Ser
NM_001257198.2:c.1278G>C	NP_001244127.1:p.Arg426Ser
NM_001257197.2:c.1062G>C	NP_001244126.1:p.Arg354Ser