Canonical Allele Identifier: CA350826948

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368387G>T (hg19) ; chr2:g.224503670G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503670G>T , CM000664.2:g.224503670G>T	GRCh38
NC_000002.11:g.225368387G>T , CM000664.1:g.225368387G>T	GRCh37
NC_000002.10:g.225076631G>T	NCBI36
NG_032169.1:g.86728C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1359C>A MANE Select	ENSP00000264414.4:p.Asn453Lys
ENST00000264414.8:c.1359C>A	ENSP00000264414.4:p.Asn453Lys
ENST00000344951.8:c.1161C>A	ENSP00000343601.4:p.Asn387Lys
ENST00000409096.5:c.1287C>A	ENSP00000387200.1:p.Asn429Lys
ENST00000409777.5:c.1287C>A	ENSP00000386525.1:p.Asn429Lys
ENST00000481135.1:n.655C>A
ENST00000617432.4:c.81C>A	ENSP00000477851.1:p.Asn27Lys
NM_001257197.1:c.1161C>A	NP_001244126.1:p.Asn387Lys
NM_001257198.1:c.1377C>A	NP_001244127.1:p.Asn459Lys
NM_003590.4:c.1359C>A	NP_003581.1:p.Asn453Lys
XM_006712800.2:c.1326C>A	XP_006712863.2:p.Asn442Lys
XM_011511994.1:c.1212C>A	XP_011510296.1:p.Asn404Lys
XM_011511995.1:c.1317C>A	XP_011510297.1:p.Asn439Lys
XM_011511996.1:c.1167C>A	XP_011510298.1:p.Asn389Lys
XM_011511997.1:c.1059C>A	XP_011510299.1:p.Asn353Lys
XM_011511994.3:c.1212C>A	XP_011510296.1:p.Asn404Lys
XM_011511996.2:c.1167C>A	XP_011510298.1:p.Asn389Lys
NM_003590.5:c.1359C>A MANE Select	NP_003581.1:p.Asn453Lys
NM_001257198.2:c.1377C>A	NP_001244127.1:p.Asn459Lys
NM_001257197.2:c.1161C>A	NP_001244126.1:p.Asn387Lys