Canonical Allele Identifier: CA1423674675

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219616G= , CM000665.2:g.179219616G=	GRCh38
NC_000003.11:g.178937404G= , CM000665.1:g.178937404G=	GRCh37
NC_000003.10:g.180420098G=	NCBI36
NG_012113.2:g.76094G= , LRG_310:g.76094G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1792G= MANE Select	ENSP00000263967.3:p.Ala598=
ENST00000462255.2:n.254G=
ENST00000643187.1:c.1792G=	ENSP00000493507.1:p.Ala598=
ENST00000674534.1:n.2700G=
ENST00000674622.1:c.213G=	ENSP00000502417.1:n.213G=
ENST00000675467.1:n.4599G=
ENST00000675786.1:c.*359G=	ENSP00000502323.1:n.*359G=
ENST00000263967.3:c.1792G=	ENSP00000263967.3:p.Ala598=
ENST00000462255.1:n.66G=
NM_006218.2:c.1792G= , LRG_310t1:c.1792G=	NP_006209.2:p.Ala598=
XM_006713658.2:c.1792G=	XP_006713721.1:p.Ala598=
XM_011512894.1:c.1792G=	XP_011511196.1:p.Ala598=
NM_006218.3:c.1792G=	NP_006209.2:p.Ala598=
XM_006713658.4:c.1792G=	XP_006713721.1:p.Ala598=
XM_011512894.2:c.1792G=	XP_011511196.1:p.Ala598=
NM_006218.4:c.1792G= MANE Select	NP_006209.2:p.Ala598=