Canonical Allele Identifier: CA16617853

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 419390
• ClinVar RCV Id: RCV000479562 ; RCV001856831
• dbSNP Id: rs1064793838
• COSMIC: COSM22541
• MyVariant Identifiers: chr3:g.178952076A>G (hg19) ; chr3:g.179234288A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234288A>G , CM000665.2:g.179234288A>G	GRCh38
NC_000003.11:g.178952076A>G , CM000665.1:g.178952076A>G	GRCh37
NC_000003.10:g.180434770A>G	NCBI36
NG_012113.2:g.90766A>G , LRG_310:g.90766A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3131A>G MANE Select	ENSP00000263967.3:p.Asn1044Ser
ENST00000462255.2:n.2154A>G
ENST00000643187.1:c.*211A>G	ENSP00000493507.1:n.*211A>G
ENST00000674534.1:n.4039A>G
ENST00000674622.1:c.1552A>G	ENSP00000502417.1:n.1552A>G
ENST00000675467.1:n.5938A>G
ENST00000675786.1:c.*1698A>G	ENSP00000502323.1:n.*1698A>G
ENST00000675796.1:n.3026A>G
ENST00000263967.3:c.3131A>G	ENSP00000263967.3:p.Asn1044Ser
NM_006218.2:c.3131A>G , LRG_310t1:c.3131A>G	NP_006209.2:p.Asn1044Ser
XM_006713658.2:c.3131A>G	XP_006713721.1:p.Asn1044Ser
XM_011512894.1:c.3131A>G	XP_011511196.1:p.Asn1044Ser
NM_006218.3:c.3131A>G	NP_006209.2:p.Asn1044Ser
XM_006713658.4:c.3131A>G	XP_006713721.1:p.Asn1044Ser
XM_011512894.2:c.3131A>G	XP_011511196.1:p.Asn1044Ser
NM_006218.4:c.3131A>G MANE Select	NP_006209.2:p.Asn1044Ser