Canonical Allele Identifier: CA16611285

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 403917
• ClinVar RCV Id: RCV000476644
• dbSNP Id: rs1060500031
• MyVariant Identifiers: chr3:g.178916940A>C (hg19) ; chr3:g.179199152A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179199152A>C , CM000665.2:g.179199152A>C	GRCh38
NC_000003.11:g.178916940A>C , CM000665.1:g.178916940A>C	GRCh37
NC_000003.10:g.180399634A>C	NCBI36
NG_012113.2:g.55630A>C , LRG_310:g.55630A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.327A>C MANE Select	ENSP00000263967.3:p.Glu109Asp
ENST00000643187.1:c.327A>C	ENSP00000493507.1:p.Glu109Asp
ENST00000675467.1:n.3134A>C
ENST00000675786.1:c.327A>C	ENSP00000502323.1:p.Glu109Asp
ENST00000263967.3:c.327A>C	ENSP00000263967.3:p.Glu109Asp
ENST00000468036.1:c.327A>C	ENSP00000417479.1:p.Glu109Asp
NM_006218.2:c.327A>C , LRG_310t1:c.327A>C	NP_006209.2:p.Glu109Asp
XM_006713658.2:c.327A>C	XP_006713721.1:p.Glu109Asp
XM_011512894.1:c.327A>C	XP_011511196.1:p.Glu109Asp
NM_006218.3:c.327A>C	NP_006209.2:p.Glu109Asp
XM_006713658.4:c.327A>C	XP_006713721.1:p.Glu109Asp
XM_011512894.2:c.327A>C	XP_011511196.1:p.Glu109Asp
NM_006218.4:c.327A>C MANE Select	NP_006209.2:p.Glu109Asp