Canonical Allele Identifier: CA355272454

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 834298
• ClinVar RCV Id: RCV001034952
• dbSNP Id: rs1724342021
• MyVariant Identifiers: chr3:g.178916887C>A (hg19) ; chr3:g.179199099C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179199099C>A , CM000665.2:g.179199099C>A	GRCh38
NC_000003.11:g.178916887C>A , CM000665.1:g.178916887C>A	GRCh37
NC_000003.10:g.180399581C>A	NCBI36
NG_012113.2:g.55577C>A , LRG_310:g.55577C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.274C>A MANE Select	ENSP00000263967.3:p.Leu92Ile
ENST00000643187.1:c.274C>A	ENSP00000493507.1:p.Leu92Ile
ENST00000675467.1:n.3081C>A
ENST00000675786.1:c.274C>A	ENSP00000502323.1:p.Leu92Ile
ENST00000263967.3:c.274C>A	ENSP00000263967.3:p.Leu92Ile
ENST00000468036.1:c.274C>A	ENSP00000417479.1:p.Leu92Ile
NM_006218.2:c.274C>A , LRG_310t1:c.274C>A	NP_006209.2:p.Leu92Ile
XM_006713658.2:c.274C>A	XP_006713721.1:p.Leu92Ile
XM_011512894.1:c.274C>A	XP_011511196.1:p.Leu92Ile
NM_006218.3:c.274C>A	NP_006209.2:p.Leu92Ile
XM_006713658.4:c.274C>A	XP_006713721.1:p.Leu92Ile
XM_011512894.2:c.274C>A	XP_011511196.1:p.Leu92Ile
NM_006218.4:c.274C>A MANE Select	NP_006209.2:p.Leu92Ile