Canonical Allele Identifier: CA1423674679

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219648T= , CM000665.2:g.179219648T=	GRCh38
NC_000003.11:g.178937436T= , CM000665.1:g.178937436T=	GRCh37
NC_000003.10:g.180420130T=	NCBI36
NG_012113.2:g.76126T= , LRG_310:g.76126T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1824T= MANE Select	ENSP00000263967.3:p.Asp608=
ENST00000462255.2:n.286T=
ENST00000643187.1:c.1824T=	ENSP00000493507.1:p.Asp608=
ENST00000674534.1:n.2732T=
ENST00000674622.1:c.245T=	ENSP00000502417.1:n.245T=
ENST00000675467.1:n.4631T=
ENST00000675786.1:c.*391T=	ENSP00000502323.1:n.*391T=
ENST00000263967.3:c.1824T=	ENSP00000263967.3:p.Asp608=
ENST00000462255.1:n.98T=
NM_006218.2:c.1824T= , LRG_310t1:c.1824T=	NP_006209.2:p.Asp608=
XM_006713658.2:c.1824T=	XP_006713721.1:p.Asp608=
XM_011512894.1:c.1824T=	XP_011511196.1:p.Asp608=
NM_006218.3:c.1824T=	NP_006209.2:p.Asp608=
XM_006713658.4:c.1824T=	XP_006713721.1:p.Asp608=
XM_011512894.2:c.1824T=	XP_011511196.1:p.Asp608=
NM_006218.4:c.1824T= MANE Select	NP_006209.2:p.Asp608=