Canonical Allele Identifier: CA355266214

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1304089
• ClinVar RCV Id: RCV001751856
• dbSNP Id: rs2108410841
• MyVariant Identifiers: chr3:g.178937419G>A (hg19) ; chr3:g.179219631G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219631G>A , CM000665.2:g.179219631G>A	GRCh38
NC_000003.11:g.178937419G>A , CM000665.1:g.178937419G>A	GRCh37
NC_000003.10:g.180420113G>A	NCBI36
NG_012113.2:g.76109G>A , LRG_310:g.76109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1807G>A MANE Select	ENSP00000263967.3:p.Asp603Asn
ENST00000462255.2:n.269G>A
ENST00000643187.1:c.1807G>A	ENSP00000493507.1:p.Asp603Asn
ENST00000674534.1:n.2715G>A
ENST00000674622.1:c.228G>A	ENSP00000502417.1:n.228G>A
ENST00000675467.1:n.4614G>A
ENST00000675786.1:c.*374G>A	ENSP00000502323.1:n.*374G>A
ENST00000263967.3:c.1807G>A	ENSP00000263967.3:p.Asp603Asn
ENST00000462255.1:n.81G>A
NM_006218.2:c.1807G>A , LRG_310t1:c.1807G>A	NP_006209.2:p.Asp603Asn
XM_006713658.2:c.1807G>A	XP_006713721.1:p.Asp603Asn
XM_011512894.1:c.1807G>A	XP_011511196.1:p.Asp603Asn
NM_006218.3:c.1807G>A	NP_006209.2:p.Asp603Asn
XM_006713658.4:c.1807G>A	XP_006713721.1:p.Asp603Asn
XM_011512894.2:c.1807G>A	XP_011511196.1:p.Asp603Asn
NM_006218.4:c.1807G>A MANE Select	NP_006209.2:p.Asp603Asn