Canonical Allele Identifier: CA2701741927
Gene: CUL3 HGNC NCBI

Linked Data

dbSNP Id: rs2106197871

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503850_224503857dup , CM000664.2:g.224503850_224503857dup GRCh38
NC_000002.11:g.225368567_225368574dup , CM000664.1:g.225368567_225368574dup GRCh37
NC_000002.10:g.225076811_225076818dup NCBI36
NG_032169.1:g.86547_86554dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1207-29_1207-22dup MANE Select ENSP00000264414.4:n.1207-29_1207-22dup
ENST00000264414.8:c.1207-29_1207-22dup ENSP00000264414.4:n.1207-29_1207-22dup
ENST00000344951.8:c.1009-29_1009-22dup ENSP00000343601.4:n.1009-29_1009-22dup
ENST00000409096.5:c.1135-29_1135-22dup ENSP00000387200.1:n.1135-29_1135-22dup
ENST00000409777.5:c.1135-29_1135-22dup ENSP00000386525.1:n.1135-29_1135-22dup
ENST00000481135.1:n.474_481dup
ENST00000617432.4:c.-70-29_-70-22dup ENSP00000477851.1:n.-70-29_-70-22dup
NM_001257197.1:c.1009-29_1009-22dup NP_001244126.1:n.1009-29_1009-22dup
NM_001257198.1:c.1225-29_1225-22dup NP_001244127.1:n.1225-29_1225-22dup
NM_003590.4:c.1207-29_1207-22dup NP_003581.1:n.1207-29_1207-22dup
XM_006712800.2:c.1174-29_1174-22dup XP_006712863.2:n.1174-29_1174-22dup
XM_011511994.1:c.1060-29_1060-22dup XP_011510296.1:n.1060-29_1060-22dup
XM_011511995.1:c.1165-29_1165-22dup XP_011510297.1:n.1165-29_1165-22dup
XM_011511996.1:c.1015-29_1015-22dup XP_011510298.1:n.1015-29_1015-22dup
XM_011511997.1:c.907-29_907-22dup XP_011510299.1:n.907-29_907-22dup
XM_011511994.3:c.1060-29_1060-22dup XP_011510296.1:n.1060-29_1060-22dup
XM_011511996.2:c.1015-29_1015-22dup XP_011510298.1:n.1015-29_1015-22dup
NM_003590.5:c.1207-29_1207-22dup MANE Select NP_003581.1:n.1207-29_1207-22dup
NM_001257198.2:c.1225-29_1225-22dup NP_001244127.1:n.1225-29_1225-22dup
NM_001257197.2:c.1009-29_1009-22dup NP_001244126.1:n.1009-29_1009-22dup