Canonical Allele Identifier: CA2663372681
Gene: CUL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224504109_224504110insCTG , CM000664.2:g.224504109_224504110insCTG GRCh38
NC_000002.11:g.225368826_225368827insCTG , CM000664.1:g.225368826_225368827insCTG GRCh37
NC_000002.10:g.225077070_225077071insCTG NCBI36
NG_032169.1:g.86288_86289insCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1207-288_1207-287insCAG MANE Select ENSP00000264414.4:n.1207-288_1207-287insCAG
ENST00000264414.8:c.1207-288_1207-287insCAG ENSP00000264414.4:n.1207-288_1207-287insCAG
ENST00000344951.8:c.1009-288_1009-287insCAG ENSP00000343601.4:n.1009-288_1009-287insCAG
ENST00000409096.5:c.1135-288_1135-287insCAG ENSP00000387200.1:n.1135-288_1135-287insCAG
ENST00000409777.5:c.1135-288_1135-287insCAG ENSP00000386525.1:n.1135-288_1135-287insCAG
ENST00000481135.1:n.215_216insCAG
ENST00000617432.4:c.-70-288_-70-287insCAG ENSP00000477851.1:n.-70-288_-70-287insCAG
NM_001257197.1:c.1009-288_1009-287insCAG NP_001244126.1:n.1009-288_1009-287insCAG
NM_001257198.1:c.1225-288_1225-287insCAG NP_001244127.1:n.1225-288_1225-287insCAG
NM_003590.4:c.1207-288_1207-287insCAG NP_003581.1:n.1207-288_1207-287insCAG
XM_006712800.2:c.1174-288_1174-287insCAG XP_006712863.2:n.1174-288_1174-287insCAG
XM_011511994.1:c.1060-288_1060-287insCAG XP_011510296.1:n.1060-288_1060-287insCAG
XM_011511995.1:c.1165-288_1165-287insCAG XP_011510297.1:n.1165-288_1165-287insCAG
XM_011511996.1:c.1015-288_1015-287insCAG XP_011510298.1:n.1015-288_1015-287insCAG
XM_011511997.1:c.907-288_907-287insCAG XP_011510299.1:n.907-288_907-287insCAG
XM_011511994.3:c.1060-288_1060-287insCAG XP_011510296.1:n.1060-288_1060-287insCAG
XM_011511996.2:c.1015-288_1015-287insCAG XP_011510298.1:n.1015-288_1015-287insCAG
NM_003590.5:c.1207-288_1207-287insCAG MANE Select NP_003581.1:n.1207-288_1207-287insCAG
NM_001257198.2:c.1225-288_1225-287insCAG NP_001244127.1:n.1225-288_1225-287insCAG
NM_001257197.2:c.1009-288_1009-287insCAG NP_001244126.1:n.1009-288_1009-287insCAG