Canonical Allele Identifier: CA16602911

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 376477
• ClinVar RCV Id: RCV000421014 ; RCV000425307 ; RCV000431720 ; RCV000431948 ; RCV000436009 ; RCV000442069 ; RCV000441979 ; RCV000442825
• dbSNP Id: rs1057519928
• COSMIC: COSM1420889 ; COSM1420890
• MyVariant Identifiers: chr3:g.178938935A>C (hg19) ; chr3:g.179221147A>C (hg38)
• PubMed: PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179221147A>C , CM000665.2:g.179221147A>C	GRCh38
NC_000003.11:g.178938935A>C , CM000665.1:g.178938935A>C	GRCh37
NC_000003.10:g.180421629A>C	NCBI36
NG_012113.2:g.77625A>C , LRG_310:g.77625A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.2177A>C MANE Select	ENSP00000263967.3:p.Glu726Ala
ENST00000462255.2:n.639A>C
ENST00000643187.1:c.2177A>C	ENSP00000493507.1:p.Glu726Ala
ENST00000674534.1:n.3085A>C
ENST00000674622.1:c.598A>C	ENSP00000502417.1:n.598A>C
ENST00000675467.1:n.4984A>C
ENST00000675786.1:c.*744A>C	ENSP00000502323.1:n.*744A>C
ENST00000263967.3:c.2177A>C	ENSP00000263967.3:p.Glu726Ala
ENST00000462255.1:n.451A>C
NM_006218.2:c.2177A>C , LRG_310t1:c.2177A>C	NP_006209.2:p.Glu726Ala
XM_006713658.2:c.2177A>C	XP_006713721.1:p.Glu726Ala
XM_011512894.1:c.2177A>C	XP_011511196.1:p.Glu726Ala
NM_006218.3:c.2177A>C	NP_006209.2:p.Glu726Ala
XM_006713658.4:c.2177A>C	XP_006713721.1:p.Glu726Ala
XM_011512894.2:c.2177A>C	XP_011511196.1:p.Glu726Ala
NM_006218.4:c.2177A>C MANE Select	NP_006209.2:p.Glu726Ala