Canonical Allele Identifier: CA437038833

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108429389
• COSMIC: COSM27130
• MyVariant Identifiers: chr3:g.178951981A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234193A>G , CM000665.2:g.179234193A>G	GRCh38
NC_000003.11:g.178951981A>G , CM000665.1:g.178951981A>G	GRCh37
NC_000003.10:g.180434675A>G	NCBI36
NG_012113.2:g.90671A>G , LRG_310:g.90671A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3036A>G MANE Select	ENSP00000263967.3:p.Glu1012=
ENST00000462255.2:n.2059A>G
ENST00000643187.1:c.*116A>G	ENSP00000493507.1:n.*116A>G
ENST00000674534.1:n.3944A>G
ENST00000674622.1:c.1457A>G	ENSP00000502417.1:n.1457A>G
ENST00000675467.1:n.5843A>G
ENST00000675786.1:c.*1603A>G	ENSP00000502323.1:n.*1603A>G
ENST00000675796.1:n.2931A>G
ENST00000263967.3:c.3036A>G	ENSP00000263967.3:p.Glu1012=
NM_006218.2:c.3036A>G , LRG_310t1:c.3036A>G	NP_006209.2:p.Glu1012=
XM_006713658.2:c.3036A>G	XP_006713721.1:p.Glu1012=
XM_011512894.1:c.3036A>G	XP_011511196.1:p.Glu1012=
NM_006218.3:c.3036A>G	NP_006209.2:p.Glu1012=
XM_006713658.4:c.3036A>G	XP_006713721.1:p.Glu1012=
XM_011512894.2:c.3036A>G	XP_011511196.1:p.Glu1012=
NM_006218.4:c.3036A>G MANE Select	NP_006209.2:p.Glu1012=