Canonical Allele Identifier: CA1331555926

Gene: CUL3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503670_224503671delinsGT , CM000664.2:g.224503670_224503671delinsGT	GRCh38
NC_000002.11:g.225368387_225368388delinsGT , CM000664.1:g.225368387_225368388delinsGT	GRCh37
NC_000002.10:g.225076631_225076632delinsGT	NCBI36
NG_032169.1:g.86727_86728delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000264414.9:c.1358_1359delinsAC MANE Select	ENSP00000264414.4:p.Asn453=
ENST00000264414.8:c.1358_1359delinsAC	ENSP00000264414.4:p.Asn453=
ENST00000344951.8:c.1160_1161delinsAC	ENSP00000343601.4:p.Asn387=
ENST00000409096.5:c.1286_1287delinsAC	ENSP00000387200.1:p.Asn429=
ENST00000409777.5:c.1286_1287delinsAC	ENSP00000386525.1:p.Asn429=
ENST00000481135.1:n.654_655delinsAC
ENST00000617432.4:c.80_81delinsAC	ENSP00000477851.1:p.Asn27=
NM_001257197.1:c.1160_1161delinsAC	NP_001244126.1:p.Asn387=
NM_001257198.1:c.1376_1377delinsAC	NP_001244127.1:p.Asn459=
NM_003590.4:c.1358_1359delinsAC	NP_003581.1:p.Asn453=
XM_006712800.2:c.1325_1326delinsAC	XP_006712863.2:p.Asn442=
XM_011511994.1:c.1211_1212delinsAC	XP_011510296.1:p.Asn404=
XM_011511995.1:c.1316_1317delinsAC	XP_011510297.1:p.Asn439=
XM_011511996.1:c.1166_1167delinsAC	XP_011510298.1:p.Asn389=
XM_011511997.1:c.1058_1059delinsAC	XP_011510299.1:p.Asn353=
XM_011511994.3:c.1211_1212delinsAC	XP_011510296.1:p.Asn404=
XM_011511996.2:c.1166_1167delinsAC	XP_011510298.1:p.Asn389=
NM_003590.5:c.1358_1359delinsAC MANE Select	NP_003581.1:p.Asn453=
NM_001257198.2:c.1376_1377delinsAC	NP_001244127.1:p.Asn459=
NM_001257197.2:c.1160_1161delinsAC	NP_001244126.1:p.Asn387=