Canonical Allele Identifier: CA1423674665

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219583G= , CM000665.2:g.179219583G=	GRCh38
NC_000003.11:g.178937371G= , CM000665.1:g.178937371G=	GRCh37
NC_000003.10:g.180420065G=	NCBI36
NG_012113.2:g.76061G= , LRG_310:g.76061G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1759G= MANE Select	ENSP00000263967.3:p.Val587=
ENST00000462255.2:n.221G=
ENST00000643187.1:c.1759G=	ENSP00000493507.1:p.Val587=
ENST00000674534.1:n.2667G=
ENST00000674622.1:c.180G=	ENSP00000502417.1:p.Trp60=
ENST00000675467.1:n.4566G=
ENST00000675786.1:c.*326G=	ENSP00000502323.1:n.*326G=
ENST00000263967.3:c.1759G=	ENSP00000263967.3:p.Val587=
ENST00000462255.1:n.33G=
NM_006218.2:c.1759G= , LRG_310t1:c.1759G=	NP_006209.2:p.Val587=
XM_006713658.2:c.1759G=	XP_006713721.1:p.Val587=
XM_011512894.1:c.1759G=	XP_011511196.1:p.Val587=
NM_006218.3:c.1759G=	NP_006209.2:p.Val587=
XM_006713658.4:c.1759G=	XP_006713721.1:p.Val587=
XM_011512894.2:c.1759G=	XP_011511196.1:p.Val587=
NM_006218.4:c.1759G= MANE Select	NP_006209.2:p.Val587=