Canonical Allele Identifier: CA1423676452

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234289T= , CM000665.2:g.179234289T=	GRCh38
NC_000003.11:g.178952077T= , CM000665.1:g.178952077T=	GRCh37
NC_000003.10:g.180434771T=	NCBI36
NG_012113.2:g.90767T= , LRG_310:g.90767T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3132T= MANE Select	ENSP00000263967.3:p.Asn1044=
ENST00000462255.2:n.2155T=
ENST00000643187.1:c.*212T=	ENSP00000493507.1:n.*212T=
ENST00000674534.1:n.4040T=
ENST00000674622.1:c.1553T=	ENSP00000502417.1:n.1553T=
ENST00000675467.1:n.5939T=
ENST00000675786.1:c.*1699T=	ENSP00000502323.1:n.*1699T=
ENST00000675796.1:n.3027T=
ENST00000263967.3:c.3132T=	ENSP00000263967.3:p.Asn1044=
NM_006218.2:c.3132T= , LRG_310t1:c.3132T=	NP_006209.2:p.Asn1044=
XM_006713658.2:c.3132T=	XP_006713721.1:p.Asn1044=
XM_011512894.1:c.3132T=	XP_011511196.1:p.Asn1044=
NM_006218.3:c.3132T=	NP_006209.2:p.Asn1044=
XM_006713658.4:c.3132T=	XP_006713721.1:p.Asn1044=
XM_011512894.2:c.3132T=	XP_011511196.1:p.Asn1044=
NM_006218.4:c.3132T= MANE Select	NP_006209.2:p.Asn1044=