Canonical Allele Identifier: CA1423676430

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234212A= , CM000665.2:g.179234212A=	GRCh38
NC_000003.11:g.178952000A= , CM000665.1:g.178952000A=	GRCh37
NC_000003.10:g.180434694A=	NCBI36
NG_012113.2:g.90690A= , LRG_310:g.90690A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3055A= MANE Select	ENSP00000263967.3:p.Ile1019=
ENST00000462255.2:n.2078A=
ENST00000643187.1:c.*135A=	ENSP00000493507.1:n.*135A=
ENST00000674534.1:n.3963A=
ENST00000674622.1:c.1476A=	ENSP00000502417.1:n.1476A=
ENST00000675467.1:n.5862A=
ENST00000675786.1:c.*1622A=	ENSP00000502323.1:n.*1622A=
ENST00000675796.1:n.2950A=
ENST00000263967.3:c.3055A=	ENSP00000263967.3:p.Ile1019=
NM_006218.2:c.3055A= , LRG_310t1:c.3055A=	NP_006209.2:p.Ile1019=
XM_006713658.2:c.3055A=	XP_006713721.1:p.Ile1019=
XM_011512894.1:c.3055A=	XP_011511196.1:p.Ile1019=
NM_006218.3:c.3055A=	NP_006209.2:p.Ile1019=
XM_006713658.4:c.3055A=	XP_006713721.1:p.Ile1019=
XM_011512894.2:c.3055A=	XP_011511196.1:p.Ile1019=
NM_006218.4:c.3055A= MANE Select	NP_006209.2:p.Ile1019=