Canonical Allele Identifier: CA350827463

Gene: CUL3

Linked Data

• dbSNP Id: rs1312027878
• gnomAD v4: 2-224503741-G-T
• MyVariant Identifiers: chr2:g.225368458G>T (hg19) ; chr2:g.224503741G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503741G>T , CM000664.2:g.224503741G>T	GRCh38
NC_000002.11:g.225368458G>T , CM000664.1:g.225368458G>T	GRCh37
NC_000002.10:g.225076702G>T	NCBI36
NG_032169.1:g.86657C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1288C>A MANE Select	ENSP00000264414.4:p.Arg430Ser
ENST00000264414.8:c.1288C>A	ENSP00000264414.4:p.Arg430Ser
ENST00000344951.8:c.1090C>A	ENSP00000343601.4:p.Arg364Ser
ENST00000409096.5:c.1216C>A	ENSP00000387200.1:p.Arg406Ser
ENST00000409777.5:c.1216C>A	ENSP00000386525.1:p.Arg406Ser
ENST00000481135.1:n.584C>A
ENST00000617432.4:c.12C>A	ENSP00000477851.1:p.Asn4Lys
NM_001257197.1:c.1090C>A	NP_001244126.1:p.Arg364Ser
NM_001257198.1:c.1306C>A	NP_001244127.1:p.Arg436Ser
NM_003590.4:c.1288C>A	NP_003581.1:p.Arg430Ser
XM_006712800.2:c.1255C>A	XP_006712863.2:p.Arg419Ser
XM_011511994.1:c.1141C>A	XP_011510296.1:p.Arg381Ser
XM_011511995.1:c.1246C>A	XP_011510297.1:p.Arg416Ser
XM_011511996.1:c.1096C>A	XP_011510298.1:p.Arg366Ser
XM_011511997.1:c.988C>A	XP_011510299.1:p.Arg330Ser
XM_011511994.3:c.1141C>A	XP_011510296.1:p.Arg381Ser
XM_011511996.2:c.1096C>A	XP_011510298.1:p.Arg366Ser
NM_003590.5:c.1288C>A MANE Select	NP_003581.1:p.Arg430Ser
NM_001257198.2:c.1306C>A	NP_001244127.1:p.Arg436Ser
NM_001257197.2:c.1090C>A	NP_001244126.1:p.Arg364Ser