Canonical Allele Identifier: CA437032875

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1775365
• ClinVar RCV Id: RCV002405518
• MyVariant Identifiers: chr3:g.178936024A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218236A>G , CM000665.2:g.179218236A>G	GRCh38
NC_000003.11:g.178936024A>G , CM000665.1:g.178936024A>G	GRCh37
NC_000003.10:g.180418718A>G	NCBI36
NG_012113.2:g.74714A>G , LRG_310:g.74714A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1566A>G MANE Select	ENSP00000263967.3:p.Glu522=
ENST00000462255.2:n.28A>G
ENST00000643187.1:c.1566A>G	ENSP00000493507.1:p.Glu522=
ENST00000674534.1:n.1320A>G
ENST00000674622.1:c.69A>G	ENSP00000502417.1:p.Glu23=
ENST00000675467.1:n.4373A>G
ENST00000675786.1:c.*133A>G	ENSP00000502323.1:n.*133A>G
ENST00000263967.3:c.1566A>G	ENSP00000263967.3:p.Glu522=
NM_006218.2:c.1566A>G , LRG_310t1:c.1566A>G	NP_006209.2:p.Glu522=
XM_006713658.2:c.1566A>G	XP_006713721.1:p.Glu522=
XM_011512894.1:c.1566A>G	XP_011511196.1:p.Glu522=
NM_006218.3:c.1566A>G	NP_006209.2:p.Glu522=
XM_006713658.4:c.1566A>G	XP_006713721.1:p.Glu522=
XM_011512894.2:c.1566A>G	XP_011511196.1:p.Glu522=
NM_006218.4:c.1566A>G MANE Select	NP_006209.2:p.Glu522=