Canonical Allele Identifier: CA1423660455

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179195153G= , CM000665.2:g.179195153G=	GRCh38
NC_000003.11:g.178912941G= , CM000665.1:g.178912941G=	GRCh37
NC_000003.10:g.180395635G=	NCBI36
NG_012113.2:g.51631G= , LRG_310:g.51631G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.-76-3597G= MANE Select	ENSP00000263967.3:n.-76-3597G=
ENST00000643187.1:c.-76-3597G=	ENSP00000493507.1:n.-76-3597G=
ENST00000675786.1:c.-76-3597G=	ENSP00000502323.1:n.-76-3597G=
ENST00000263967.3:c.-76-3597G=	ENSP00000263967.3:n.-76-3597G=
ENST00000468036.1:c.-76-3597G=	ENSP00000417479.1:n.-76-3597G=
ENST00000477735.1:c.-76-3597G=	ENSP00000418145.1:n.-76-3597G=
NM_006218.2:c.-76-3597G= , LRG_310t1:c.-76-3597G=	NP_006209.2:n.-76-3597G=
XM_006713658.2:c.-76-3597G=	XP_006713721.1:n.-76-3597G=
XM_011512894.1:c.-76-3597G=	XP_011511196.1:n.-76-3597G=
NM_006218.3:c.-76-3597G=	NP_006209.2:n.-76-3597G=
XM_006713658.4:c.-76-3597G=	XP_006713721.1:n.-76-3597G=
XM_011512894.2:c.-76-3597G=	XP_011511196.1:n.-76-3597G=
NM_006218.4:c.-76-3597G= MANE Select	NP_006209.2:n.-76-3597G=