Canonical Allele Identifier: CA355279269

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1725176062
• MyVariant Identifiers: chr3:g.178947800C>T (hg19) ; chr3:g.179230012C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179230012C>T , CM000665.2:g.179230012C>T	GRCh38
NC_000003.11:g.178947800C>T , CM000665.1:g.178947800C>T	GRCh37
NC_000003.10:g.180430494C>T	NCBI36
NG_012113.2:g.86490C>T , LRG_310:g.86490C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263967.4:c.2675C>T MANE Select	ENSP00000263967.3:p.Ala892Val
ENST00000462255.2:n.1698C>T
ENST00000643187.1:c.2675C>T	ENSP00000493507.1:p.Ala892Val
ENST00000674534.1:n.3583C>T
ENST00000674622.1:c.1096C>T	ENSP00000502417.1:n.1096C>T
ENST00000675467.1:n.5482C>T
ENST00000675786.1:c.*1242C>T	ENSP00000502323.1:n.*1242C>T
ENST00000675796.1:n.2570C>T
ENST00000263967.3:c.2675C>T	ENSP00000263967.3:p.Ala892Val
NM_006218.2:c.2675C>T , LRG_310t1:c.2675C>T	NP_006209.2:p.Ala892Val
XM_006713658.2:c.2675C>T	XP_006713721.1:p.Ala892Val
XM_011512894.1:c.2675C>T	XP_011511196.1:p.Ala892Val
NM_006218.3:c.2675C>T	NP_006209.2:p.Ala892Val
XM_006713658.4:c.2675C>T	XP_006713721.1:p.Ala892Val
XM_011512894.2:c.2675C>T	XP_011511196.1:p.Ala892Val
NM_006218.4:c.2675C>T MANE Select	NP_006209.2:p.Ala892Val