Canonical Allele Identifier: CA1423674652

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219558T= , CM000665.2:g.179219558T=	GRCh38
NC_000003.11:g.178937346T= , CM000665.1:g.178937346T=	GRCh37
NC_000003.10:g.180420040T=	NCBI36
NG_012113.2:g.76036T= , LRG_310:g.76036T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1747-13T= MANE Select	ENSP00000263967.3:n.1747-13T=
ENST00000462255.2:n.209-13T=
ENST00000643187.1:c.1747-13T=	ENSP00000493507.1:n.1747-13T=
ENST00000674534.1:n.2642T=
ENST00000674622.1:c.168-13T=	ENSP00000502417.1:n.168-13T=
ENST00000675467.1:n.4554-13T=
ENST00000675786.1:c.*314-13T=	ENSP00000502323.1:n.*314-13T=
ENST00000263967.3:c.1747-13T=	ENSP00000263967.3:n.1747-13T=
ENST00000462255.1:n.8T=
NM_006218.2:c.1747-13T= , LRG_310t1:c.1747-13T=	NP_006209.2:n.1747-13T=
XM_006713658.2:c.1747-13T=	XP_006713721.1:n.1747-13T=
XM_011512894.1:c.1747-13T=	XP_011511196.1:n.1747-13T=
NM_006218.3:c.1747-13T=	NP_006209.2:n.1747-13T=
XM_006713658.4:c.1747-13T=	XP_006713721.1:n.1747-13T=
XM_011512894.2:c.1747-13T=	XP_011511196.1:n.1747-13T=
NM_006218.4:c.1747-13T= MANE Select	NP_006209.2:n.1747-13T=