Canonical Allele Identifier: CA355281001
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs1204477021

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179203716T>A , CM000665.2:g.179203716T>A GRCh38
NC_000003.11:g.178921504T>A , CM000665.1:g.178921504T>A GRCh37
NC_000003.10:g.180404198T>A NCBI36
NG_012113.2:g.60194T>A , LRG_310:g.60194T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.986T>A MANE Select ENSP00000263967.3:p.Val329Asp
ENST00000643187.1:c.986T>A ENSP00000493507.1:p.Val329Asp
ENST00000674534.1:n.740T>A
ENST00000675467.1:n.3793T>A
ENST00000675786.1:c.986T>A ENSP00000502323.1:p.Val329Asp
ENST00000263967.3:c.986T>A ENSP00000263967.3:p.Val329Asp
NM_006218.2:c.986T>A , LRG_310t1:c.986T>A NP_006209.2:p.Val329Asp
XM_006713658.2:c.986T>A XP_006713721.1:p.Val329Asp
XM_011512894.1:c.986T>A XP_011511196.1:p.Val329Asp
NM_006218.3:c.986T>A NP_006209.2:p.Val329Asp
XM_006713658.4:c.986T>A XP_006713721.1:p.Val329Asp
XM_011512894.2:c.986T>A XP_011511196.1:p.Val329Asp
NM_006218.4:c.986T>A MANE Select NP_006209.2:p.Val329Asp