Canonical Allele Identifier: CA350826955

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368389T>A (hg19) ; chr2:g.224503672T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503672T>A , CM000664.2:g.224503672T>A	GRCh38
NC_000002.11:g.225368389T>A , CM000664.1:g.225368389T>A	GRCh37
NC_000002.10:g.225076633T>A	NCBI36
NG_032169.1:g.86726A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1357A>T MANE Select	ENSP00000264414.4:p.Asn453Tyr
ENST00000264414.8:c.1357A>T	ENSP00000264414.4:p.Asn453Tyr
ENST00000344951.8:c.1159A>T	ENSP00000343601.4:p.Asn387Tyr
ENST00000409096.5:c.1285A>T	ENSP00000387200.1:p.Asn429Tyr
ENST00000409777.5:c.1285A>T	ENSP00000386525.1:p.Asn429Tyr
ENST00000481135.1:n.653A>T
ENST00000617432.4:c.79A>T	ENSP00000477851.1:p.Asn27Tyr
NM_001257197.1:c.1159A>T	NP_001244126.1:p.Asn387Tyr
NM_001257198.1:c.1375A>T	NP_001244127.1:p.Asn459Tyr
NM_003590.4:c.1357A>T	NP_003581.1:p.Asn453Tyr
XM_006712800.2:c.1324A>T	XP_006712863.2:p.Asn442Tyr
XM_011511994.1:c.1210A>T	XP_011510296.1:p.Asn404Tyr
XM_011511995.1:c.1315A>T	XP_011510297.1:p.Asn439Tyr
XM_011511996.1:c.1165A>T	XP_011510298.1:p.Asn389Tyr
XM_011511997.1:c.1057A>T	XP_011510299.1:p.Asn353Tyr
XM_011511994.3:c.1210A>T	XP_011510296.1:p.Asn404Tyr
XM_011511996.2:c.1165A>T	XP_011510298.1:p.Asn389Tyr
NM_003590.5:c.1357A>T MANE Select	NP_003581.1:p.Asn453Tyr
NM_001257198.2:c.1375A>T	NP_001244127.1:p.Asn459Tyr
NM_001257197.2:c.1159A>T	NP_001244126.1:p.Asn387Tyr