Canonical Allele Identifier: CA2663372691

Gene: CUL3

Linked Data

• gnomAD v4: 2-224504132-AATTTTAGTCACAGAGATTATTTTATGAAGCCTTTGCATATGCAGGCAAAAACTTACACAGCCAAAAGACGGAATTTTTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224504137_224504215del , CM000664.2:g.224504137_224504215del	GRCh38
NC_000002.11:g.225368854_225368932del , CM000664.1:g.225368854_225368932del	GRCh37
NC_000002.10:g.225077098_225077176del	NCBI36
NG_032169.1:g.86187_86265del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1207-389_1207-311del MANE Select	ENSP00000264414.4:n.1207-389_1207-311del
ENST00000264414.8:c.1207-389_1207-311del	ENSP00000264414.4:n.1207-389_1207-311del
ENST00000344951.8:c.1009-389_1009-311del	ENSP00000343601.4:n.1009-389_1009-311del
ENST00000409096.5:c.1135-389_1135-311del	ENSP00000387200.1:n.1135-389_1135-311del
ENST00000409777.5:c.1135-389_1135-311del	ENSP00000386525.1:n.1135-389_1135-311del
ENST00000481135.1:n.114_192del
ENST00000617432.4:c.-70-389_-70-311del	ENSP00000477851.1:n.-70-389_-70-311del
NM_001257197.1:c.1009-389_1009-311del	NP_001244126.1:n.1009-389_1009-311del
NM_001257198.1:c.1225-389_1225-311del	NP_001244127.1:n.1225-389_1225-311del
NM_003590.4:c.1207-389_1207-311del	NP_003581.1:n.1207-389_1207-311del
XM_006712800.2:c.1174-389_1174-311del	XP_006712863.2:n.1174-389_1174-311del
XM_011511994.1:c.1060-389_1060-311del	XP_011510296.1:n.1060-389_1060-311del
XM_011511995.1:c.1165-389_1165-311del	XP_011510297.1:n.1165-389_1165-311del
XM_011511996.1:c.1015-389_1015-311del	XP_011510298.1:n.1015-389_1015-311del
XM_011511997.1:c.907-389_907-311del	XP_011510299.1:n.907-389_907-311del
XM_011511994.3:c.1060-389_1060-311del	XP_011510296.1:n.1060-389_1060-311del
XM_011511996.2:c.1015-389_1015-311del	XP_011510298.1:n.1015-389_1015-311del
NM_003590.5:c.1207-389_1207-311del MANE Select	NP_003581.1:n.1207-389_1207-311del
NM_001257198.2:c.1225-389_1225-311del	NP_001244127.1:n.1225-389_1225-311del
NM_001257197.2:c.1009-389_1009-311del	NP_001244126.1:n.1009-389_1009-311del