Canonical Allele Identifier: CA355285195

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178951982C>A (hg19) ; chr3:g.179234194C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234194C>A , CM000665.2:g.179234194C>A	GRCh38
NC_000003.11:g.178951982C>A , CM000665.1:g.178951982C>A	GRCh37
NC_000003.10:g.180434676C>A	NCBI36
NG_012113.2:g.90672C>A , LRG_310:g.90672C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3037C>A MANE Select	ENSP00000263967.3:p.Leu1013Ile
ENST00000462255.2:n.2060C>A
ENST00000643187.1:c.*117C>A	ENSP00000493507.1:n.*117C>A
ENST00000674534.1:n.3945C>A
ENST00000674622.1:c.1458C>A	ENSP00000502417.1:n.1458C>A
ENST00000675467.1:n.5844C>A
ENST00000675786.1:c.*1604C>A	ENSP00000502323.1:n.*1604C>A
ENST00000675796.1:n.2932C>A
ENST00000263967.3:c.3037C>A	ENSP00000263967.3:p.Leu1013Ile
NM_006218.2:c.3037C>A , LRG_310t1:c.3037C>A	NP_006209.2:p.Leu1013Ile
XM_006713658.2:c.3037C>A	XP_006713721.1:p.Leu1013Ile
XM_011512894.1:c.3037C>A	XP_011511196.1:p.Leu1013Ile
NM_006218.3:c.3037C>A	NP_006209.2:p.Leu1013Ile
XM_006713658.4:c.3037C>A	XP_006713721.1:p.Leu1013Ile
XM_011512894.2:c.3037C>A	XP_011511196.1:p.Leu1013Ile
NM_006218.4:c.3037C>A MANE Select	NP_006209.2:p.Leu1013Ile