Canonical Allele Identifier: CA1423676413

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234142C= , CM000665.2:g.179234142C=	GRCh38
NC_000003.11:g.178951930C= , CM000665.1:g.178951930C=	GRCh37
NC_000003.10:g.180434624C=	NCBI36
NG_012113.2:g.90620C= , LRG_310:g.90620C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.2985C= MANE Select	ENSP00000263967.3:p.Ala995=
ENST00000462255.2:n.2008C=
ENST00000643187.1:c.*65C=	ENSP00000493507.1:n.*65C=
ENST00000674534.1:n.3893C=
ENST00000674622.1:c.1406C=	ENSP00000502417.1:n.1406C=
ENST00000675467.1:n.5792C=
ENST00000675786.1:c.*1552C=	ENSP00000502323.1:n.*1552C=
ENST00000675796.1:n.2880C=
ENST00000263967.3:c.2985C=	ENSP00000263967.3:p.Ala995=
NM_006218.2:c.2985C= , LRG_310t1:c.2985C=	NP_006209.2:p.Ala995=
XM_006713658.2:c.2985C=	XP_006713721.1:p.Ala995=
XM_011512894.1:c.2985C=	XP_011511196.1:p.Ala995=
NM_006218.3:c.2985C=	NP_006209.2:p.Ala995=
XM_006713658.4:c.2985C=	XP_006713721.1:p.Ala995=
XM_011512894.2:c.2985C=	XP_011511196.1:p.Ala995=
NM_006218.4:c.2985C= MANE Select	NP_006209.2:p.Ala995=