Canonical Allele Identifier: CA355280559

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1724480380
• gnomAD v4: 3-179203670-G-A
• MyVariant Identifiers: chr3:g.178921458G>A (hg19) ; chr3:g.179203670G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179203670G>A , CM000665.2:g.179203670G>A	GRCh38
NC_000003.11:g.178921458G>A , CM000665.1:g.178921458G>A	GRCh37
NC_000003.10:g.180404152G>A	NCBI36
NG_012113.2:g.60148G>A , LRG_310:g.60148G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.940G>A MANE Select	ENSP00000263967.3:p.Ala314Thr
ENST00000643187.1:c.940G>A	ENSP00000493507.1:p.Ala314Thr
ENST00000674534.1:n.694G>A
ENST00000675467.1:n.3747G>A
ENST00000675786.1:c.940G>A	ENSP00000502323.1:p.Ala314Thr
ENST00000263967.3:c.940G>A	ENSP00000263967.3:p.Ala314Thr
NM_006218.2:c.940G>A , LRG_310t1:c.940G>A	NP_006209.2:p.Ala314Thr
XM_006713658.2:c.940G>A	XP_006713721.1:p.Ala314Thr
XM_011512894.1:c.940G>A	XP_011511196.1:p.Ala314Thr
NM_006218.3:c.940G>A	NP_006209.2:p.Ala314Thr
XM_006713658.4:c.940G>A	XP_006713721.1:p.Ala314Thr
XM_011512894.2:c.940G>A	XP_011511196.1:p.Ala314Thr
NM_006218.4:c.940G>A MANE Select	NP_006209.2:p.Ala314Thr