Canonical Allele Identifier: CA355265821

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1467831050
• gnomAD v2: 3-178937371-G-A
• gnomAD v4: 3-179219583-G-A
• MyVariant Identifiers: chr3:g.178937371G>A (hg19) ; chr3:g.179219583G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219583G>A , CM000665.2:g.179219583G>A	GRCh38
NC_000003.11:g.178937371G>A , CM000665.1:g.178937371G>A	GRCh37
NC_000003.10:g.180420065G>A	NCBI36
NG_012113.2:g.76061G>A , LRG_310:g.76061G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1759G>A MANE Select	ENSP00000263967.3:p.Val587Ile
ENST00000462255.2:n.221G>A
ENST00000643187.1:c.1759G>A	ENSP00000493507.1:p.Val587Ile
ENST00000674534.1:n.2667G>A
ENST00000674622.1:c.180G>A	ENSP00000502417.1:p.Trp60Ter
ENST00000675467.1:n.4566G>A
ENST00000675786.1:c.*326G>A	ENSP00000502323.1:n.*326G>A
ENST00000263967.3:c.1759G>A	ENSP00000263967.3:p.Val587Ile
ENST00000462255.1:n.33G>A
NM_006218.2:c.1759G>A , LRG_310t1:c.1759G>A	NP_006209.2:p.Val587Ile
XM_006713658.2:c.1759G>A	XP_006713721.1:p.Val587Ile
XM_011512894.1:c.1759G>A	XP_011511196.1:p.Val587Ile
NM_006218.3:c.1759G>A	NP_006209.2:p.Val587Ile
XM_006713658.4:c.1759G>A	XP_006713721.1:p.Val587Ile
XM_011512894.2:c.1759G>A	XP_011511196.1:p.Val587Ile
NM_006218.4:c.1759G>A MANE Select	NP_006209.2:p.Val587Ile