Canonical Allele Identifier: CA350826917

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368380A>C (hg19) ; chr2:g.224503663A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503663A>C , CM000664.2:g.224503663A>C	GRCh38
NC_000002.11:g.225368380A>C , CM000664.1:g.225368380A>C	GRCh37
NC_000002.10:g.225076624A>C	NCBI36
NG_032169.1:g.86735T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1366T>G MANE Select	ENSP00000264414.4:p.Ser456Ala
ENST00000264414.8:c.1366T>G	ENSP00000264414.4:p.Ser456Ala
ENST00000344951.8:c.1168T>G	ENSP00000343601.4:p.Ser390Ala
ENST00000409096.5:c.1294T>G	ENSP00000387200.1:p.Ser432Ala
ENST00000409777.5:c.1294T>G	ENSP00000386525.1:p.Ser432Ala
ENST00000481135.1:n.662T>G
ENST00000617432.4:c.88T>G	ENSP00000477851.1:p.Ser30Ala
NM_001257197.1:c.1168T>G	NP_001244126.1:p.Ser390Ala
NM_001257198.1:c.1384T>G	NP_001244127.1:p.Ser462Ala
NM_003590.4:c.1366T>G	NP_003581.1:p.Ser456Ala
XM_006712800.2:c.1333T>G	XP_006712863.2:p.Ser445Ala
XM_011511994.1:c.1219T>G	XP_011510296.1:p.Ser407Ala
XM_011511995.1:c.1324T>G	XP_011510297.1:p.Ser442Ala
XM_011511996.1:c.1174T>G	XP_011510298.1:p.Ser392Ala
XM_011511997.1:c.1066T>G	XP_011510299.1:p.Ser356Ala
XM_011511994.3:c.1219T>G	XP_011510296.1:p.Ser407Ala
XM_011511996.2:c.1174T>G	XP_011510298.1:p.Ser392Ala
NM_003590.5:c.1366T>G MANE Select	NP_003581.1:p.Ser456Ala
NM_001257198.2:c.1384T>G	NP_001244127.1:p.Ser462Ala
NM_001257197.2:c.1168T>G	NP_001244126.1:p.Ser390Ala