Canonical Allele Identifier: CA437033064

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1787574
• ClinVar RCV Id: RCV002425679
• MyVariant Identifiers: chr3:g.178916634A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179198846A>C , CM000665.2:g.179198846A>C	GRCh38
NC_000003.11:g.178916634A>C , CM000665.1:g.178916634A>C	GRCh37
NC_000003.10:g.180399328A>C	NCBI36
NG_012113.2:g.55324A>C , LRG_310:g.55324A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.21A>C MANE Select	ENSP00000263967.3:p.Ser7=
ENST00000643187.1:c.21A>C	ENSP00000493507.1:p.Ser7=
ENST00000675467.1:n.2828A>C
ENST00000675786.1:c.21A>C	ENSP00000502323.1:p.Ser7=
ENST00000263967.3:c.21A>C	ENSP00000263967.3:p.Ser7=
ENST00000468036.1:c.21A>C	ENSP00000417479.1:p.Ser7=
ENST00000477735.1:c.21A>C	ENSP00000418145.1:p.Ser7=
NM_006218.2:c.21A>C , LRG_310t1:c.21A>C	NP_006209.2:p.Ser7=
XM_006713658.2:c.21A>C	XP_006713721.1:p.Ser7=
XM_011512894.1:c.21A>C	XP_011511196.1:p.Ser7=
NM_006218.3:c.21A>C	NP_006209.2:p.Ser7=
XM_006713658.4:c.21A>C	XP_006713721.1:p.Ser7=
XM_011512894.2:c.21A>C	XP_011511196.1:p.Ser7=
NM_006218.4:c.21A>C MANE Select	NP_006209.2:p.Ser7=