Canonical Allele Identifier: CA1423674132

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218215C= , CM000665.2:g.179218215C=	GRCh38
NC_000003.11:g.178936003C= , CM000665.1:g.178936003C=	GRCh37
NC_000003.10:g.180418697C=	NCBI36
NG_012113.2:g.74693C= , LRG_310:g.74693C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1545C= MANE Select	ENSP00000263967.3:p.Asn515=
ENST00000462255.2:n.7C=
ENST00000643187.1:c.1545C=	ENSP00000493507.1:p.Asn515=
ENST00000674534.1:n.1299C=
ENST00000674622.1:c.48C=	ENSP00000502417.1:p.Asn16=
ENST00000675467.1:n.4352C=
ENST00000675786.1:c.*112C=	ENSP00000502323.1:n.*112C=
ENST00000263967.3:c.1545C=	ENSP00000263967.3:p.Asn515=
NM_006218.2:c.1545C= , LRG_310t1:c.1545C=	NP_006209.2:p.Asn515=
XM_006713658.2:c.1545C=	XP_006713721.1:p.Asn515=
XM_011512894.1:c.1545C=	XP_011511196.1:p.Asn515=
NM_006218.3:c.1545C=	NP_006209.2:p.Asn515=
XM_006713658.4:c.1545C=	XP_006713721.1:p.Asn515=
XM_011512894.2:c.1545C=	XP_011511196.1:p.Asn515=
NM_006218.4:c.1545C= MANE Select	NP_006209.2:p.Asn515=