Canonical Allele Identifier: CA2701739853

Gene: CUL3

Linked Data

• dbSNP Id: rs2106197332

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503775_224503776del , CM000664.2:g.224503775_224503776del	GRCh38
NC_000002.11:g.225368492_225368493del , CM000664.1:g.225368492_225368493del	GRCh37
NC_000002.10:g.225076736_225076737del	NCBI36
NG_032169.1:g.86625_86626del

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1256_1257del MANE Select	ENSP00000264414.4:p.Phe419Ter
ENST00000264414.8:c.1256_1257del	ENSP00000264414.4:p.Phe419Ter
ENST00000344951.8:c.1058_1059del	ENSP00000343601.4:p.Phe353Ter
ENST00000409096.5:c.1184_1185del	ENSP00000387200.1:p.Phe395Ter
ENST00000409777.5:c.1184_1185del	ENSP00000386525.1:p.Phe395Ter
ENST00000481135.1:n.552_553del
ENST00000617432.4:c.-21_-20del	ENSP00000477851.1:n.-21_-20del
NM_001257197.1:c.1058_1059del	NP_001244126.1:p.Phe353Ter
NM_001257198.1:c.1274_1275del	NP_001244127.1:p.Phe425Ter
NM_003590.4:c.1256_1257del	NP_003581.1:p.Phe419Ter
XM_006712800.2:c.1223_1224del	XP_006712863.2:p.Phe408Ter
XM_011511994.1:c.1109_1110del	XP_011510296.1:p.Phe370Ter
XM_011511995.1:c.1214_1215del	XP_011510297.1:p.Phe405Ter
XM_011511996.1:c.1064_1065del	XP_011510298.1:p.Phe355Ter
XM_011511997.1:c.956_957del	XP_011510299.1:p.Phe319Ter
XM_011511994.3:c.1109_1110del	XP_011510296.1:p.Phe370Ter
XM_011511996.2:c.1064_1065del	XP_011510298.1:p.Phe355Ter
NM_003590.5:c.1256_1257del MANE Select	NP_003581.1:p.Phe419Ter
NM_001257198.2:c.1274_1275del	NP_001244127.1:p.Phe425Ter
NM_001257197.2:c.1058_1059del	NP_001244126.1:p.Phe353Ter