Canonical Allele Identifier: CA437038982

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 747570
• ClinVar RCV Id: RCV000924291
• dbSNP Id: rs1576949990
• MyVariant Identifiers: chr3:g.178952095C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234307C>A , CM000665.2:g.179234307C>A	GRCh38
NC_000003.11:g.178952095C>A , CM000665.1:g.178952095C>A	GRCh37
NC_000003.10:g.180434789C>A	NCBI36
NG_012113.2:g.90785C>A , LRG_310:g.90785C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.3150C>A MANE Select	ENSP00000263967.3:p.Gly1050=
ENST00000462255.2:n.2173C>A
ENST00000643187.1:c.*230C>A	ENSP00000493507.1:n.*230C>A
ENST00000674534.1:n.4058C>A
ENST00000674622.1:c.1571C>A	ENSP00000502417.1:n.1571C>A
ENST00000675467.1:n.5957C>A
ENST00000675786.1:c.*1717C>A	ENSP00000502323.1:n.*1717C>A
ENST00000675796.1:n.3045C>A
ENST00000263967.3:c.3150C>A	ENSP00000263967.3:p.Gly1050=
NM_006218.2:c.3150C>A , LRG_310t1:c.3150C>A	NP_006209.2:p.Gly1050=
XM_006713658.2:c.3150C>A	XP_006713721.1:p.Gly1050=
XM_011512894.1:c.3150C>A	XP_011511196.1:p.Gly1050=
NM_006218.3:c.3150C>A	NP_006209.2:p.Gly1050=
XM_006713658.4:c.3150C>A	XP_006713721.1:p.Gly1050=
XM_011512894.2:c.3150C>A	XP_011511196.1:p.Gly1050=
NM_006218.4:c.3150C>A MANE Select	NP_006209.2:p.Gly1050=