Canonical Allele Identifier: CA765436976

Gene: CUL3

Linked Data

• dbSNP Id: rs749647898
• MyVariant Identifiers: chr2:g.225368683_225368684del (hg19) ; chr2:g.224503966_224503967del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503967_224503968del , CM000664.2:g.224503967_224503968del	GRCh38
NC_000002.11:g.225368684_225368685del , CM000664.1:g.225368684_225368685del	GRCh37
NC_000002.10:g.225076928_225076929del	NCBI36
NG_032169.1:g.86431_86432del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1207-145_1207-144del MANE Select	ENSP00000264414.4:n.1207-145_1207-144del
ENST00000264414.8:c.1207-145_1207-144del	ENSP00000264414.4:n.1207-145_1207-144del
ENST00000344951.8:c.1009-145_1009-144del	ENSP00000343601.4:n.1009-145_1009-144del
ENST00000409096.5:c.1135-145_1135-144del	ENSP00000387200.1:n.1135-145_1135-144del
ENST00000409777.5:c.1135-145_1135-144del	ENSP00000386525.1:n.1135-145_1135-144del
ENST00000481135.1:n.358_359del
ENST00000617432.4:c.-70-145_-70-144del	ENSP00000477851.1:n.-70-145_-70-144del
NM_001257197.1:c.1009-145_1009-144del	NP_001244126.1:n.1009-145_1009-144del
NM_001257198.1:c.1225-145_1225-144del	NP_001244127.1:n.1225-145_1225-144del
NM_003590.4:c.1207-145_1207-144del	NP_003581.1:n.1207-145_1207-144del
XM_006712800.2:c.1174-145_1174-144del	XP_006712863.2:n.1174-145_1174-144del
XM_011511994.1:c.1060-145_1060-144del	XP_011510296.1:n.1060-145_1060-144del
XM_011511995.1:c.1165-145_1165-144del	XP_011510297.1:n.1165-145_1165-144del
XM_011511996.1:c.1015-145_1015-144del	XP_011510298.1:n.1015-145_1015-144del
XM_011511997.1:c.907-145_907-144del	XP_011510299.1:n.907-145_907-144del
XM_011511994.3:c.1060-145_1060-144del	XP_011510296.1:n.1060-145_1060-144del
XM_011511996.2:c.1015-145_1015-144del	XP_011510298.1:n.1015-145_1015-144del
NM_003590.5:c.1207-145_1207-144del MANE Select	NP_003581.1:n.1207-145_1207-144del
NM_001257198.2:c.1225-145_1225-144del	NP_001244127.1:n.1225-145_1225-144del
NM_001257197.2:c.1009-145_1009-144del	NP_001244126.1:n.1009-145_1009-144del