Canonical Allele Identifier: CA350826960

Gene: CUL3

Linked Data

• MyVariant Identifiers: chr2:g.225368390T>A (hg19) ; chr2:g.224503673T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503673T>A , CM000664.2:g.224503673T>A	GRCh38
NC_000002.11:g.225368390T>A , CM000664.1:g.225368390T>A	GRCh37
NC_000002.10:g.225076634T>A	NCBI36
NG_032169.1:g.86725A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1356A>T MANE Select	ENSP00000264414.4:p.Lys452Asn
ENST00000264414.8:c.1356A>T	ENSP00000264414.4:p.Lys452Asn
ENST00000344951.8:c.1158A>T	ENSP00000343601.4:p.Lys386Asn
ENST00000409096.5:c.1284A>T	ENSP00000387200.1:p.Lys428Asn
ENST00000409777.5:c.1284A>T	ENSP00000386525.1:p.Lys428Asn
ENST00000481135.1:n.652A>T
ENST00000617432.4:c.79-1A>T	ENSP00000477851.1:n.79-1A>T
NM_001257197.1:c.1158A>T	NP_001244126.1:p.Lys386Asn
NM_001257198.1:c.1374A>T	NP_001244127.1:p.Lys458Asn
NM_003590.4:c.1356A>T	NP_003581.1:p.Lys452Asn
XM_006712800.2:c.1323A>T	XP_006712863.2:p.Lys441Asn
XM_011511994.1:c.1209A>T	XP_011510296.1:p.Lys403Asn
XM_011511995.1:c.1314A>T	XP_011510297.1:p.Lys438Asn
XM_011511996.1:c.1164A>T	XP_011510298.1:p.Lys388Asn
XM_011511997.1:c.1056A>T	XP_011510299.1:p.Lys352Asn
XM_011511994.3:c.1209A>T	XP_011510296.1:p.Lys403Asn
XM_011511996.2:c.1164A>T	XP_011510298.1:p.Lys388Asn
NM_003590.5:c.1356A>T MANE Select	NP_003581.1:p.Lys452Asn
NM_001257198.2:c.1374A>T	NP_001244127.1:p.Lys458Asn
NM_001257197.2:c.1158A>T	NP_001244126.1:p.Lys386Asn