Canonical Allele Identifier: CA355264627

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1724885947
• gnomAD v4: 3-179218232-A-G
• COSMIC: COSM29121
• MyVariant Identifiers: chr3:g.178936020A>G (hg19) ; chr3:g.179218232A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218232A>G , CM000665.2:g.179218232A>G	GRCh38
NC_000003.11:g.178936020A>G , CM000665.1:g.178936020A>G	GRCh37
NC_000003.10:g.180418714A>G	NCBI36
NG_012113.2:g.74710A>G , LRG_310:g.74710A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1562A>G MANE Select	ENSP00000263967.3:p.Asn521Ser
ENST00000462255.2:n.24A>G
ENST00000643187.1:c.1562A>G	ENSP00000493507.1:p.Asn521Ser
ENST00000674534.1:n.1316A>G
ENST00000674622.1:c.65A>G	ENSP00000502417.1:p.Asn22Ser
ENST00000675467.1:n.4369A>G
ENST00000675786.1:c.*129A>G	ENSP00000502323.1:n.*129A>G
ENST00000263967.3:c.1562A>G	ENSP00000263967.3:p.Asn521Ser
NM_006218.2:c.1562A>G , LRG_310t1:c.1562A>G	NP_006209.2:p.Asn521Ser
XM_006713658.2:c.1562A>G	XP_006713721.1:p.Asn521Ser
XM_011512894.1:c.1562A>G	XP_011511196.1:p.Asn521Ser
NM_006218.3:c.1562A>G	NP_006209.2:p.Asn521Ser
XM_006713658.4:c.1562A>G	XP_006713721.1:p.Asn521Ser
XM_011512894.2:c.1562A>G	XP_011511196.1:p.Asn521Ser
NM_006218.4:c.1562A>G MANE Select	NP_006209.2:p.Asn521Ser