Canonical Allele Identifier: CA355281001

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1204477021
• gnomAD v2: 3-178921504-T-A
• gnomAD v4: 3-179203716-T-A
• MyVariant Identifiers: chr3:g.178921504T>A (hg19) ; chr3:g.179203716T>A (hg38)

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