Canonical Allele Identifier: CA1423674678

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219645A= , CM000665.2:g.179219645A=	GRCh38
NC_000003.11:g.178937433A= , CM000665.1:g.178937433A=	GRCh37
NC_000003.10:g.180420127A=	NCBI36
NG_012113.2:g.76123A= , LRG_310:g.76123A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1821A= MANE Select	ENSP00000263967.3:p.Pro607=
ENST00000462255.2:n.283A=
ENST00000643187.1:c.1821A=	ENSP00000493507.1:p.Pro607=
ENST00000674534.1:n.2729A=
ENST00000674622.1:c.242A=	ENSP00000502417.1:n.242A=
ENST00000675467.1:n.4628A=
ENST00000675786.1:c.*388A=	ENSP00000502323.1:n.*388A=
ENST00000263967.3:c.1821A=	ENSP00000263967.3:p.Pro607=
ENST00000462255.1:n.95A=
NM_006218.2:c.1821A= , LRG_310t1:c.1821A=	NP_006209.2:p.Pro607=
XM_006713658.2:c.1821A=	XP_006713721.1:p.Pro607=
XM_011512894.1:c.1821A=	XP_011511196.1:p.Pro607=
NM_006218.3:c.1821A=	NP_006209.2:p.Pro607=
XM_006713658.4:c.1821A=	XP_006713721.1:p.Pro607=
XM_011512894.2:c.1821A=	XP_011511196.1:p.Pro607=
NM_006218.4:c.1821A= MANE Select	NP_006209.2:p.Pro607=