Canonical Allele Identifier: CA350830494

Gene: CUL3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224511498G>A , CM000664.2:g.224511498G>A	GRCh38
NC_000002.11:g.225376215G>A , CM000664.1:g.225376215G>A	GRCh37
NC_000002.10:g.225084459G>A	NCBI36
NG_032169.1:g.78900C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.739C>T MANE Select	ENSP00000264414.4:p.Arg247Ter
ENST00000264414.8:c.739C>T	ENSP00000264414.4:p.Arg247Ter
ENST00000344951.8:c.541C>T	ENSP00000343601.4:p.Arg181Ter
ENST00000409096.5:c.667C>T	ENSP00000387200.1:p.Arg223Ter
ENST00000409777.5:c.667C>T	ENSP00000386525.1:p.Arg223Ter
ENST00000541548.5:n.475C>T
NM_001257197.1:c.541C>T	NP_001244126.1:p.Arg181Ter
NM_001257198.1:c.757C>T	NP_001244127.1:p.Arg253Ter
NM_003590.4:c.739C>T	NP_003581.1:p.Arg247Ter
XM_006712800.2:c.706C>T	XP_006712863.2:p.Arg236Ter
XM_011511994.1:c.592C>T	XP_011510296.1:p.Arg198Ter
XM_011511995.1:c.697C>T	XP_011510297.1:p.Arg233Ter
XM_011511996.1:c.547C>T	XP_011510298.1:p.Arg183Ter
XM_011511997.1:c.439C>T	XP_011510299.1:p.Arg147Ter
XM_011511994.3:c.592C>T	XP_011510296.1:p.Arg198Ter
XM_011511996.2:c.547C>T	XP_011510298.1:p.Arg183Ter
NM_003590.5:c.739C>T MANE Select	NP_003581.1:p.Arg247Ter
NM_001257198.2:c.757C>T	NP_001244127.1:p.Arg253Ter
NM_001257197.2:c.541C>T	NP_001244126.1:p.Arg181Ter