Canonical Allele Identifier: CA88527179

Gene: PIK3CA

Linked Data

• dbSNP Id: rs988134846
• gnomAD v2: 3-178936109-C-G
• MyVariant Identifiers: chr3:g.178936109C>G (hg19) ; chr3:g.179218321C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218321C>G , CM000665.2:g.179218321C>G	GRCh38
NC_000003.11:g.178936109C>G , CM000665.1:g.178936109C>G	GRCh37
NC_000003.10:g.180418803C>G	NCBI36
NG_012113.2:g.74799C>G , LRG_310:g.74799C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1651C>G MANE Select	ENSP00000263967.3:p.Leu551Val
ENST00000462255.2:n.113C>G
ENST00000643187.1:c.1651C>G	ENSP00000493507.1:p.Leu551Val
ENST00000674534.1:n.1405C>G
ENST00000674622.1:c.154C>G	ENSP00000502417.1:p.Leu52Val
ENST00000675467.1:n.4458C>G
ENST00000675786.1:c.*218C>G	ENSP00000502323.1:n.*218C>G
ENST00000263967.3:c.1651C>G	ENSP00000263967.3:p.Leu551Val
NM_006218.2:c.1651C>G , LRG_310t1:c.1651C>G	NP_006209.2:p.Leu551Val
XM_006713658.2:c.1651C>G	XP_006713721.1:p.Leu551Val
XM_011512894.1:c.1651C>G	XP_011511196.1:p.Leu551Val
NM_006218.3:c.1651C>G	NP_006209.2:p.Leu551Val
XM_006713658.4:c.1651C>G	XP_006713721.1:p.Leu551Val
XM_011512894.2:c.1651C>G	XP_011511196.1:p.Leu551Val
NM_006218.4:c.1651C>G MANE Select	NP_006209.2:p.Leu551Val