Canonical Allele Identifier: CA1423669313

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179229996C= , CM000665.2:g.179229996C=	GRCh38
NC_000003.11:g.178947784C= , CM000665.1:g.178947784C=	GRCh37
NC_000003.10:g.180430478C=	NCBI36
NG_012113.2:g.86474C= , LRG_310:g.86474C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.2667-8C= MANE Select	ENSP00000263967.3:n.2667-8C=
ENST00000462255.2:n.1682C=
ENST00000643187.1:c.2667-8C=	ENSP00000493507.1:n.2667-8C=
ENST00000674534.1:n.3575-8C=
ENST00000674622.1:c.1088-8C=	ENSP00000502417.1:n.1088-8C=
ENST00000675467.1:n.5474-8C=
ENST00000675786.1:c.*1234-8C=	ENSP00000502323.1:n.*1234-8C=
ENST00000675796.1:n.2562-8C=
ENST00000263967.3:c.2667-8C=	ENSP00000263967.3:n.2667-8C=
NM_006218.2:c.2667-8C= , LRG_310t1:c.2667-8C=	NP_006209.2:n.2667-8C=
XM_006713658.2:c.2667-8C=	XP_006713721.1:n.2667-8C=
XM_011512894.1:c.2667-8C=	XP_011511196.1:n.2667-8C=
NM_006218.3:c.2667-8C=	NP_006209.2:n.2667-8C=
XM_006713658.4:c.2667-8C=	XP_006713721.1:n.2667-8C=
XM_011512894.2:c.2667-8C=	XP_011511196.1:n.2667-8C=
NM_006218.4:c.2667-8C= MANE Select	NP_006209.2:n.2667-8C=