Canonical Allele Identifier: CA350827544

Gene: CUL3

Linked Data

• gnomAD v4: 2-224503762-G-T
• MyVariant Identifiers: chr2:g.225368479G>T (hg19) ; chr2:g.224503762G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.224503762G>T , CM000664.2:g.224503762G>T	GRCh38
NC_000002.11:g.225368479G>T , CM000664.1:g.225368479G>T	GRCh37
NC_000002.10:g.225076723G>T	NCBI36
NG_032169.1:g.86636C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264414.9:c.1267C>A MANE Select	ENSP00000264414.4:p.Gln423Lys
ENST00000264414.8:c.1267C>A	ENSP00000264414.4:p.Gln423Lys
ENST00000344951.8:c.1069C>A	ENSP00000343601.4:p.Gln357Lys
ENST00000409096.5:c.1195C>A	ENSP00000387200.1:p.Gln399Lys
ENST00000409777.5:c.1195C>A	ENSP00000386525.1:p.Gln399Lys
ENST00000481135.1:n.563C>A
ENST00000617432.4:c.-10C>A	ENSP00000477851.1:n.-10C>A
NM_001257197.1:c.1069C>A	NP_001244126.1:p.Gln357Lys
NM_001257198.1:c.1285C>A	NP_001244127.1:p.Gln429Lys
NM_003590.4:c.1267C>A	NP_003581.1:p.Gln423Lys
XM_006712800.2:c.1234C>A	XP_006712863.2:p.Gln412Lys
XM_011511994.1:c.1120C>A	XP_011510296.1:p.Gln374Lys
XM_011511995.1:c.1225C>A	XP_011510297.1:p.Gln409Lys
XM_011511996.1:c.1075C>A	XP_011510298.1:p.Gln359Lys
XM_011511997.1:c.967C>A	XP_011510299.1:p.Gln323Lys
XM_011511994.3:c.1120C>A	XP_011510296.1:p.Gln374Lys
XM_011511996.2:c.1075C>A	XP_011510298.1:p.Gln359Lys
NM_003590.5:c.1267C>A MANE Select	NP_003581.1:p.Gln423Lys
NM_001257198.2:c.1285C>A	NP_001244127.1:p.Gln429Lys
NM_001257197.2:c.1069C>A	NP_001244126.1:p.Gln357Lys