Canonical Allele Identifier: CA437038863

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1725280697
• MyVariant Identifiers: chr3:g.178952005A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234217A>C , CM000665.2:g.179234217A>C	GRCh38
NC_000003.11:g.178952005A>C , CM000665.1:g.178952005A>C	GRCh37
NC_000003.10:g.180434699A>C	NCBI36
NG_012113.2:g.90695A>C , LRG_310:g.90695A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3060A>C MANE Select	ENSP00000263967.3:p.Ala1020=
ENST00000462255.2:n.2083A>C
ENST00000643187.1:c.*140A>C	ENSP00000493507.1:n.*140A>C
ENST00000674534.1:n.3968A>C
ENST00000674622.1:c.1481A>C	ENSP00000502417.1:n.1481A>C
ENST00000675467.1:n.5867A>C
ENST00000675786.1:c.*1627A>C	ENSP00000502323.1:n.*1627A>C
ENST00000675796.1:n.2955A>C
ENST00000263967.3:c.3060A>C	ENSP00000263967.3:p.Ala1020=
NM_006218.2:c.3060A>C , LRG_310t1:c.3060A>C	NP_006209.2:p.Ala1020=
XM_006713658.2:c.3060A>C	XP_006713721.1:p.Ala1020=
XM_011512894.1:c.3060A>C	XP_011511196.1:p.Ala1020=
NM_006218.3:c.3060A>C	NP_006209.2:p.Ala1020=
XM_006713658.4:c.3060A>C	XP_006713721.1:p.Ala1020=
XM_011512894.2:c.3060A>C	XP_011511196.1:p.Ala1020=
NM_006218.4:c.3060A>C MANE Select	NP_006209.2:p.Ala1020=