Canonical Allele Identifier: CA1423676431

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234213T= , CM000665.2:g.179234213T=	GRCh38
NC_000003.11:g.178952001T= , CM000665.1:g.178952001T=	GRCh37
NC_000003.10:g.180434695T=	NCBI36
NG_012113.2:g.90691T= , LRG_310:g.90691T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3056T= MANE Select	ENSP00000263967.3:p.Ile1019=
ENST00000462255.2:n.2079T=
ENST00000643187.1:c.*136T=	ENSP00000493507.1:n.*136T=
ENST00000674534.1:n.3964T=
ENST00000674622.1:c.1477T=	ENSP00000502417.1:n.1477T=
ENST00000675467.1:n.5863T=
ENST00000675786.1:c.*1623T=	ENSP00000502323.1:n.*1623T=
ENST00000675796.1:n.2951T=
ENST00000263967.3:c.3056T=	ENSP00000263967.3:p.Ile1019=
NM_006218.2:c.3056T= , LRG_310t1:c.3056T=	NP_006209.2:p.Ile1019=
XM_006713658.2:c.3056T=	XP_006713721.1:p.Ile1019=
XM_011512894.1:c.3056T=	XP_011511196.1:p.Ile1019=
NM_006218.3:c.3056T=	NP_006209.2:p.Ile1019=
XM_006713658.4:c.3056T=	XP_006713721.1:p.Ile1019=
XM_011512894.2:c.3056T=	XP_011511196.1:p.Ile1019=
NM_006218.4:c.3056T= MANE Select	NP_006209.2:p.Ile1019=