Canonical Allele Identifier: CA16602926

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 376494
• ClinVar RCV Id: RCV000421528 ; RCV000424314 ; RCV000430901 ; RCV000431544 ; RCV000438739 ; RCV000441606
• dbSNP Id: rs749415085
• COSMIC: COSM87310 ; COSM1041447
• MyVariant Identifiers: chr3:g.178916725C>A (hg19) ; chr3:g.179198937C>A (hg38)
• PubMed: PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179198937C>A , CM000665.2:g.179198937C>A	GRCh38
NC_000003.11:g.178916725C>A , CM000665.1:g.178916725C>A	GRCh37
NC_000003.10:g.180399419C>A	NCBI36
NG_012113.2:g.55415C>A , LRG_310:g.55415C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.112C>A MANE Select	ENSP00000263967.3:p.Arg38Ser
ENST00000643187.1:c.112C>A	ENSP00000493507.1:p.Arg38Ser
ENST00000675467.1:n.2919C>A
ENST00000675786.1:c.112C>A	ENSP00000502323.1:p.Arg38Ser
ENST00000263967.3:c.112C>A	ENSP00000263967.3:p.Arg38Ser
ENST00000468036.1:c.112C>A	ENSP00000417479.1:p.Arg38Ser
NM_006218.2:c.112C>A , LRG_310t1:c.112C>A	NP_006209.2:p.Arg38Ser
XM_006713658.2:c.112C>A	XP_006713721.1:p.Arg38Ser
XM_011512894.1:c.112C>A	XP_011511196.1:p.Arg38Ser
NM_006218.3:c.112C>A	NP_006209.2:p.Arg38Ser
XM_006713658.4:c.112C>A	XP_006713721.1:p.Arg38Ser
XM_011512894.2:c.112C>A	XP_011511196.1:p.Arg38Ser
NM_006218.4:c.112C>A MANE Select	NP_006209.2:p.Arg38Ser