Canonical Allele Identifier: CA539863250

Gene: CUL3

Linked Data

• dbSNP Id: rs1379505709
• gnomAD v2: 2-225368567-AT-A
• gnomAD v4: 2-224503850-AT-A
• MyVariant Identifiers: chr2:g.225368568del (hg19) ; chr2:g.224503851del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503851del , CM000664.2:g.224503851del	GRCh38
NC_000002.11:g.225368568del , CM000664.1:g.225368568del	GRCh37
NC_000002.10:g.225076812del	NCBI36
NG_032169.1:g.86547del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1207-29del MANE Select	ENSP00000264414.4:n.1207-29del
ENST00000264414.8:c.1207-29del	ENSP00000264414.4:n.1207-29del
ENST00000344951.8:c.1009-29del	ENSP00000343601.4:n.1009-29del
ENST00000409096.5:c.1135-29del	ENSP00000387200.1:n.1135-29del
ENST00000409777.5:c.1135-29del	ENSP00000386525.1:n.1135-29del
ENST00000481135.1:n.474del
ENST00000617432.4:c.-70-29del	ENSP00000477851.1:n.-70-29del
NM_001257197.1:c.1009-29del	NP_001244126.1:n.1009-29del
NM_001257198.1:c.1225-29del	NP_001244127.1:n.1225-29del
NM_003590.4:c.1207-29del	NP_003581.1:n.1207-29del
XM_006712800.2:c.1174-29del	XP_006712863.2:n.1174-29del
XM_011511994.1:c.1060-29del	XP_011510296.1:n.1060-29del
XM_011511995.1:c.1165-29del	XP_011510297.1:n.1165-29del
XM_011511996.1:c.1015-29del	XP_011510298.1:n.1015-29del
XM_011511997.1:c.907-29del	XP_011510299.1:n.907-29del
XM_011511994.3:c.1060-29del	XP_011510296.1:n.1060-29del
XM_011511996.2:c.1015-29del	XP_011510298.1:n.1015-29del
NM_003590.5:c.1207-29del MANE Select	NP_003581.1:n.1207-29del
NM_001257198.2:c.1225-29del	NP_001244127.1:n.1225-29del
NM_001257197.2:c.1009-29del	NP_001244126.1:n.1009-29del