Canonical Allele Identifier: CA1423676462

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234302G= , CM000665.2:g.179234302G=	GRCh38
NC_000003.11:g.178952090G= , CM000665.1:g.178952090G=	GRCh37
NC_000003.10:g.180434784G=	NCBI36
NG_012113.2:g.90780G= , LRG_310:g.90780G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3145G= MANE Select	ENSP00000263967.3:p.Gly1049=
ENST00000462255.2:n.2168G=
ENST00000643187.1:c.*225G=	ENSP00000493507.1:n.*225G=
ENST00000674534.1:n.4053G=
ENST00000674622.1:c.1566G=	ENSP00000502417.1:n.1566G=
ENST00000675467.1:n.5952G=
ENST00000675786.1:c.*1712G=	ENSP00000502323.1:n.*1712G=
ENST00000675796.1:n.3040G=
ENST00000263967.3:c.3145G=	ENSP00000263967.3:p.Gly1049=
NM_006218.2:c.3145G= , LRG_310t1:c.3145G=	NP_006209.2:p.Gly1049=
XM_006713658.2:c.3145G=	XP_006713721.1:p.Gly1049=
XM_011512894.1:c.3145G=	XP_011511196.1:p.Gly1049=
NM_006218.3:c.3145G=	NP_006209.2:p.Gly1049=
XM_006713658.4:c.3145G=	XP_006713721.1:p.Gly1049=
XM_011512894.2:c.3145G=	XP_011511196.1:p.Gly1049=
NM_006218.4:c.3145G= MANE Select	NP_006209.2:p.Gly1049=