Canonical Allele Identifier: CA350826951

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368388T>C (hg19) ; chr2:g.224503671T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503671T>C , CM000664.2:g.224503671T>C	GRCh38
NC_000002.11:g.225368388T>C , CM000664.1:g.225368388T>C	GRCh37
NC_000002.10:g.225076632T>C	NCBI36
NG_032169.1:g.86727A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1358A>G MANE Select	ENSP00000264414.4:p.Asn453Ser
ENST00000264414.8:c.1358A>G	ENSP00000264414.4:p.Asn453Ser
ENST00000344951.8:c.1160A>G	ENSP00000343601.4:p.Asn387Ser
ENST00000409096.5:c.1286A>G	ENSP00000387200.1:p.Asn429Ser
ENST00000409777.5:c.1286A>G	ENSP00000386525.1:p.Asn429Ser
ENST00000481135.1:n.654A>G
ENST00000617432.4:c.80A>G	ENSP00000477851.1:p.Asn27Ser
NM_001257197.1:c.1160A>G	NP_001244126.1:p.Asn387Ser
NM_001257198.1:c.1376A>G	NP_001244127.1:p.Asn459Ser
NM_003590.4:c.1358A>G	NP_003581.1:p.Asn453Ser
XM_006712800.2:c.1325A>G	XP_006712863.2:p.Asn442Ser
XM_011511994.1:c.1211A>G	XP_011510296.1:p.Asn404Ser
XM_011511995.1:c.1316A>G	XP_011510297.1:p.Asn439Ser
XM_011511996.1:c.1166A>G	XP_011510298.1:p.Asn389Ser
XM_011511997.1:c.1058A>G	XP_011510299.1:p.Asn353Ser
XM_011511994.3:c.1211A>G	XP_011510296.1:p.Asn404Ser
XM_011511996.2:c.1166A>G	XP_011510298.1:p.Asn389Ser
NM_003590.5:c.1358A>G MANE Select	NP_003581.1:p.Asn453Ser
NM_001257198.2:c.1376A>G	NP_001244127.1:p.Asn459Ser
NM_001257197.2:c.1160A>G	NP_001244126.1:p.Asn387Ser