Canonical Allele Identifier: CA431492566

Gene: CUL3

Linked Data

• dbSNP Id: rs2106196553
• MyVariant Identifiers: chr2:g.225368387G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1359C>T MANE Select	ENSP00000264414.4:p.Asn453=
ENST00000264414.8:c.1359C>T	ENSP00000264414.4:p.Asn453=
ENST00000344951.8:c.1161C>T	ENSP00000343601.4:p.Asn387=
ENST00000409096.5:c.1287C>T	ENSP00000387200.1:p.Asn429=
ENST00000409777.5:c.1287C>T	ENSP00000386525.1:p.Asn429=
ENST00000481135.1:n.655C>T
ENST00000617432.4:c.81C>T	ENSP00000477851.1:p.Asn27=
NM_001257197.1:c.1161C>T	NP_001244126.1:p.Asn387=
NM_001257198.1:c.1377C>T	NP_001244127.1:p.Asn459=
NM_003590.4:c.1359C>T	NP_003581.1:p.Asn453=
XM_006712800.2:c.1326C>T	XP_006712863.2:p.Asn442=
XM_011511994.1:c.1212C>T	XP_011510296.1:p.Asn404=
XM_011511995.1:c.1317C>T	XP_011510297.1:p.Asn439=
XM_011511996.1:c.1167C>T	XP_011510298.1:p.Asn389=
XM_011511997.1:c.1059C>T	XP_011510299.1:p.Asn353=
XM_011511994.3:c.1212C>T	XP_011510296.1:p.Asn404=
XM_011511996.2:c.1167C>T	XP_011510298.1:p.Asn389=
NM_003590.5:c.1359C>T MANE Select	NP_003581.1:p.Asn453=
NM_001257198.2:c.1377C>T	NP_001244127.1:p.Asn459=
NM_001257197.2:c.1161C>T	NP_001244126.1:p.Asn387=