Canonical Allele Identifier: CA437038829

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178951978A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234190A>C , CM000665.2:g.179234190A>C	GRCh38
NC_000003.11:g.178951978A>C , CM000665.1:g.178951978A>C	GRCh37
NC_000003.10:g.180434672A>C	NCBI36
NG_012113.2:g.90668A>C , LRG_310:g.90668A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3033A>C MANE Select	ENSP00000263967.3:p.Pro1011=
ENST00000462255.2:n.2056A>C
ENST00000643187.1:c.*113A>C	ENSP00000493507.1:n.*113A>C
ENST00000674534.1:n.3941A>C
ENST00000674622.1:c.1454A>C	ENSP00000502417.1:n.1454A>C
ENST00000675467.1:n.5840A>C
ENST00000675786.1:c.*1600A>C	ENSP00000502323.1:n.*1600A>C
ENST00000675796.1:n.2928A>C
ENST00000263967.3:c.3033A>C	ENSP00000263967.3:p.Pro1011=
NM_006218.2:c.3033A>C , LRG_310t1:c.3033A>C	NP_006209.2:p.Pro1011=
XM_006713658.2:c.3033A>C	XP_006713721.1:p.Pro1011=
XM_011512894.1:c.3033A>C	XP_011511196.1:p.Pro1011=
NM_006218.3:c.3033A>C	NP_006209.2:p.Pro1011=
XM_006713658.4:c.3033A>C	XP_006713721.1:p.Pro1011=
XM_011512894.2:c.3033A>C	XP_011511196.1:p.Pro1011=
NM_006218.4:c.3033A>C MANE Select	NP_006209.2:p.Pro1011=