Canonical Allele Identifier: CA1423674672

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219598C= , CM000665.2:g.179219598C=	GRCh38
NC_000003.11:g.178937386C= , CM000665.1:g.178937386C=	GRCh37
NC_000003.10:g.180420080C=	NCBI36
NG_012113.2:g.76076C= , LRG_310:g.76076C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1774C= MANE Select	ENSP00000263967.3:p.Pro592=
ENST00000462255.2:n.236C=
ENST00000643187.1:c.1774C=	ENSP00000493507.1:p.Pro592=
ENST00000674534.1:n.2682C=
ENST00000674622.1:c.195C=	ENSP00000502417.1:n.195C=
ENST00000675467.1:n.4581C=
ENST00000675786.1:c.*341C=	ENSP00000502323.1:n.*341C=
ENST00000263967.3:c.1774C=	ENSP00000263967.3:p.Pro592=
ENST00000462255.1:n.48C=
NM_006218.2:c.1774C= , LRG_310t1:c.1774C=	NP_006209.2:p.Pro592=
XM_006713658.2:c.1774C=	XP_006713721.1:p.Pro592=
XM_011512894.1:c.1774C=	XP_011511196.1:p.Pro592=
NM_006218.3:c.1774C=	NP_006209.2:p.Pro592=
XM_006713658.4:c.1774C=	XP_006713721.1:p.Pro592=
XM_011512894.2:c.1774C=	XP_011511196.1:p.Pro592=
NM_006218.4:c.1774C= MANE Select	NP_006209.2:p.Pro592=