Canonical Allele Identifier: CA1331555992
Gene: CUL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.224503897T= , CM000664.2:g.224503897T= GRCh38
NC_000002.11:g.225368614T= , CM000664.1:g.225368614T= GRCh37
NC_000002.10:g.225076858T= NCBI36
NG_032169.1:g.86501A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264414.9:c.1207-75A= MANE Select ENSP00000264414.4:n.1207-75A=
ENST00000264414.8:c.1207-75A= ENSP00000264414.4:n.1207-75A=
ENST00000344951.8:c.1009-75A= ENSP00000343601.4:n.1009-75A=
ENST00000409096.5:c.1135-75A= ENSP00000387200.1:n.1135-75A=
ENST00000409777.5:c.1135-75A= ENSP00000386525.1:n.1135-75A=
ENST00000481135.1:n.428A=
ENST00000617432.4:c.-70-75A= ENSP00000477851.1:n.-70-75A=
NM_001257197.1:c.1009-75A= NP_001244126.1:n.1009-75A=
NM_001257198.1:c.1225-75A= NP_001244127.1:n.1225-75A=
NM_003590.4:c.1207-75A= NP_003581.1:n.1207-75A=
XM_006712800.2:c.1174-75A= XP_006712863.2:n.1174-75A=
XM_011511994.1:c.1060-75A= XP_011510296.1:n.1060-75A=
XM_011511995.1:c.1165-75A= XP_011510297.1:n.1165-75A=
XM_011511996.1:c.1015-75A= XP_011510298.1:n.1015-75A=
XM_011511997.1:c.907-75A= XP_011510299.1:n.907-75A=
XM_011511994.3:c.1060-75A= XP_011510296.1:n.1060-75A=
XM_011511996.2:c.1015-75A= XP_011510298.1:n.1015-75A=
NM_003590.5:c.1207-75A= MANE Select NP_003581.1:n.1207-75A=
NM_001257198.2:c.1225-75A= NP_001244127.1:n.1225-75A=
NM_001257197.2:c.1009-75A= NP_001244126.1:n.1009-75A=