Canonical Allele Identifier: CA355266507

Gene: PIK3CA

Linked Data

• MyVariant Identifiers: chr3:g.178937450G>A (hg19) ; chr3:g.179219662G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179219662G>A , CM000665.2:g.179219662G>A	GRCh38
NC_000003.11:g.178937450G>A , CM000665.1:g.178937450G>A	GRCh37
NC_000003.10:g.180420144G>A	NCBI36
NG_012113.2:g.76140G>A , LRG_310:g.76140G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.1838G>A MANE Select	ENSP00000263967.3:p.Gly613Asp
ENST00000462255.2:n.300G>A
ENST00000643187.1:c.1838G>A	ENSP00000493507.1:p.Gly613Asp
ENST00000674534.1:n.2746G>A
ENST00000674622.1:c.259G>A	ENSP00000502417.1:n.259G>A
ENST00000675467.1:n.4645G>A
ENST00000675786.1:c.*405G>A	ENSP00000502323.1:n.*405G>A
ENST00000263967.3:c.1838G>A	ENSP00000263967.3:p.Gly613Asp
ENST00000462255.1:n.112G>A
NM_006218.2:c.1838G>A , LRG_310t1:c.1838G>A	NP_006209.2:p.Gly613Asp
XM_006713658.2:c.1838G>A	XP_006713721.1:p.Gly613Asp
XM_011512894.1:c.1838G>A	XP_011511196.1:p.Gly613Asp
NM_006218.3:c.1838G>A	NP_006209.2:p.Gly613Asp
XM_006713658.4:c.1838G>A	XP_006713721.1:p.Gly613Asp
XM_011512894.2:c.1838G>A	XP_011511196.1:p.Gly613Asp
NM_006218.4:c.1838G>A MANE Select	NP_006209.2:p.Gly613Asp