Canonical Allele Identifier: CA2663372668
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224504095_224504096insTGC , CM000664.2:g.224504095_224504096insTGC GRCh38
NC_000002.11:g.225368812_225368813insTGC , CM000664.1:g.225368812_225368813insTGC GRCh37
NC_000002.10:g.225077056_225077057insTGC NCBI36
NG_032169.1:g.86304_86305insAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1207-272_1207-271insAGC MANE Select ENSP00000264414.4:n.1207-272_1207-271insAGC
ENST00000264414.8:c.1207-272_1207-271insAGC ENSP00000264414.4:n.1207-272_1207-271insAGC
ENST00000344951.8:c.1009-272_1009-271insAGC ENSP00000343601.4:n.1009-272_1009-271insAGC
ENST00000409096.5:c.1135-272_1135-271insAGC ENSP00000387200.1:n.1135-272_1135-271insAGC
ENST00000409777.5:c.1135-272_1135-271insAGC ENSP00000386525.1:n.1135-272_1135-271insAGC
ENST00000481135.1:n.231_232insAGC
ENST00000617432.4:c.-70-272_-70-271insAGC ENSP00000477851.1:n.-70-272_-70-271insAGC
NM_001257197.1:c.1009-272_1009-271insAGC NP_001244126.1:n.1009-272_1009-271insAGC
NM_001257198.1:c.1225-272_1225-271insAGC NP_001244127.1:n.1225-272_1225-271insAGC
NM_003590.4:c.1207-272_1207-271insAGC NP_003581.1:n.1207-272_1207-271insAGC
XM_006712800.2:c.1174-272_1174-271insAGC XP_006712863.2:n.1174-272_1174-271insAGC
XM_011511994.1:c.1060-272_1060-271insAGC XP_011510296.1:n.1060-272_1060-271insAGC
XM_011511995.1:c.1165-272_1165-271insAGC XP_011510297.1:n.1165-272_1165-271insAGC
XM_011511996.1:c.1015-272_1015-271insAGC XP_011510298.1:n.1015-272_1015-271insAGC
XM_011511997.1:c.907-272_907-271insAGC XP_011510299.1:n.907-272_907-271insAGC
XM_011511994.3:c.1060-272_1060-271insAGC XP_011510296.1:n.1060-272_1060-271insAGC
XM_011511996.2:c.1015-272_1015-271insAGC XP_011510298.1:n.1015-272_1015-271insAGC
NM_003590.5:c.1207-272_1207-271insAGC MANE Select NP_003581.1:n.1207-272_1207-271insAGC
NM_001257198.2:c.1225-272_1225-271insAGC NP_001244127.1:n.1225-272_1225-271insAGC
NM_001257197.2:c.1009-272_1009-271insAGC NP_001244126.1:n.1009-272_1009-271insAGC