Canonical Allele Identifier: CA914560615
Gene: CUL3 HGNC NCBI

Linked Data

dbSNP Id: rs1559144061

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224504170_224504172dup , CM000664.2:g.224504170_224504172dup GRCh38
NC_000002.11:g.225368887_225368889dup , CM000664.1:g.225368887_225368889dup GRCh37
NC_000002.10:g.225077131_225077133dup NCBI36
NG_032169.1:g.86226_86228dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1207-350_1207-348dup MANE Select ENSP00000264414.4:n.1207-350_1207-348dup
ENST00000264414.8:c.1207-350_1207-348dup ENSP00000264414.4:n.1207-350_1207-348dup
ENST00000344951.8:c.1009-350_1009-348dup ENSP00000343601.4:n.1009-350_1009-348dup
ENST00000409096.5:c.1135-350_1135-348dup ENSP00000387200.1:n.1135-350_1135-348dup
ENST00000409777.5:c.1135-350_1135-348dup ENSP00000386525.1:n.1135-350_1135-348dup
ENST00000481135.1:n.153_155dup
ENST00000617432.4:c.-70-350_-70-348dup ENSP00000477851.1:n.-70-350_-70-348dup
NM_001257197.1:c.1009-350_1009-348dup NP_001244126.1:n.1009-350_1009-348dup
NM_001257198.1:c.1225-350_1225-348dup NP_001244127.1:n.1225-350_1225-348dup
NM_003590.4:c.1207-350_1207-348dup NP_003581.1:n.1207-350_1207-348dup
XM_006712800.2:c.1174-350_1174-348dup XP_006712863.2:n.1174-350_1174-348dup
XM_011511994.1:c.1060-350_1060-348dup XP_011510296.1:n.1060-350_1060-348dup
XM_011511995.1:c.1165-350_1165-348dup XP_011510297.1:n.1165-350_1165-348dup
XM_011511996.1:c.1015-350_1015-348dup XP_011510298.1:n.1015-350_1015-348dup
XM_011511997.1:c.907-350_907-348dup XP_011510299.1:n.907-350_907-348dup
XM_011511994.3:c.1060-350_1060-348dup XP_011510296.1:n.1060-350_1060-348dup
XM_011511996.2:c.1015-350_1015-348dup XP_011510298.1:n.1015-350_1015-348dup
NM_003590.5:c.1207-350_1207-348dup MANE Select NP_003581.1:n.1207-350_1207-348dup
NM_001257198.2:c.1225-350_1225-348dup NP_001244127.1:n.1225-350_1225-348dup
NM_001257197.2:c.1009-350_1009-348dup NP_001244126.1:n.1009-350_1009-348dup