Canonical Allele Identifier: CA10584687

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 246683
• ClinVar RCV Id: RCV001457698 ; RCV003298311
• dbSNP Id: rs879254355
• gnomAD v4: 3-179199038-A-G
• MyVariant Identifiers: chr3:g.178916826A>G (hg19) ; chr3:g.179199038A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179199038A>G , CM000665.2:g.179199038A>G	GRCh38
NC_000003.11:g.178916826A>G , CM000665.1:g.178916826A>G	GRCh37
NC_000003.10:g.180399520A>G	NCBI36
NG_012113.2:g.55516A>G , LRG_310:g.55516A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.213A>G MANE Select	ENSP00000263967.3:p.Val71=
ENST00000643187.1:c.213A>G	ENSP00000493507.1:p.Val71=
ENST00000675467.1:n.3020A>G
ENST00000675786.1:c.213A>G	ENSP00000502323.1:p.Val71=
ENST00000263967.3:c.213A>G	ENSP00000263967.3:p.Val71=
ENST00000468036.1:c.213A>G	ENSP00000417479.1:p.Val71=
NM_006218.2:c.213A>G , LRG_310t1:c.213A>G	NP_006209.2:p.Val71=
XM_006713658.2:c.213A>G	XP_006713721.1:p.Val71=
XM_011512894.1:c.213A>G	XP_011511196.1:p.Val71=
NM_006218.3:c.213A>G	NP_006209.2:p.Val71=
XM_006713658.4:c.213A>G	XP_006713721.1:p.Val71=
XM_011512894.2:c.213A>G	XP_011511196.1:p.Val71=
NM_006218.4:c.213A>G MANE Select	NP_006209.2:p.Val71=