Canonical Allele Identifier: CA437032905

Gene: PIK3CA

Linked Data

• ClinVar Variation Id: 1776522
• ClinVar RCV Id: RCV002394868
• dbSNP Id: rs2108408258
• MyVariant Identifiers: chr3:g.178936075T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179218287T>A , CM000665.2:g.179218287T>A	GRCh38
NC_000003.11:g.178936075T>A , CM000665.1:g.178936075T>A	GRCh37
NC_000003.10:g.180418769T>A	NCBI36
NG_012113.2:g.74765T>A , LRG_310:g.74765T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1617T>A MANE Select	ENSP00000263967.3:p.Pro539=
ENST00000462255.2:n.79T>A
ENST00000643187.1:c.1617T>A	ENSP00000493507.1:p.Pro539=
ENST00000674534.1:n.1371T>A
ENST00000674622.1:c.120T>A	ENSP00000502417.1:p.Pro40=
ENST00000675467.1:n.4424T>A
ENST00000675786.1:c.*184T>A	ENSP00000502323.1:n.*184T>A
ENST00000263967.3:c.1617T>A	ENSP00000263967.3:p.Pro539=
NM_006218.2:c.1617T>A , LRG_310t1:c.1617T>A	NP_006209.2:p.Pro539=
XM_006713658.2:c.1617T>A	XP_006713721.1:p.Pro539=
XM_011512894.1:c.1617T>A	XP_011511196.1:p.Pro539=
NM_006218.3:c.1617T>A	NP_006209.2:p.Pro539=
XM_006713658.4:c.1617T>A	XP_006713721.1:p.Pro539=
XM_011512894.2:c.1617T>A	XP_011511196.1:p.Pro539=
NM_006218.4:c.1617T>A MANE Select	NP_006209.2:p.Pro539=