Canonical Allele Identifier: CA1423676438

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234244T= , CM000665.2:g.179234244T=	GRCh38
NC_000003.11:g.178952032T= , CM000665.1:g.178952032T=	GRCh37
NC_000003.10:g.180434726T=	NCBI36
NG_012113.2:g.90722T= , LRG_310:g.90722T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3087T= MANE Select	ENSP00000263967.3:p.Asp1029=
ENST00000462255.2:n.2110T=
ENST00000643187.1:c.*167T=	ENSP00000493507.1:n.*167T=
ENST00000674534.1:n.3995T=
ENST00000674622.1:c.1508T=	ENSP00000502417.1:n.1508T=
ENST00000675467.1:n.5894T=
ENST00000675786.1:c.*1654T=	ENSP00000502323.1:n.*1654T=
ENST00000675796.1:n.2982T=
ENST00000263967.3:c.3087T=	ENSP00000263967.3:p.Asp1029=
NM_006218.2:c.3087T= , LRG_310t1:c.3087T=	NP_006209.2:p.Asp1029=
XM_006713658.2:c.3087T=	XP_006713721.1:p.Asp1029=
XM_011512894.1:c.3087T=	XP_011511196.1:p.Asp1029=
NM_006218.3:c.3087T=	NP_006209.2:p.Asp1029=
XM_006713658.4:c.3087T=	XP_006713721.1:p.Asp1029=
XM_011512894.2:c.3087T=	XP_011511196.1:p.Asp1029=
NM_006218.4:c.3087T= MANE Select	NP_006209.2:p.Asp1029=