Canonical Allele Identifier: CA437038968

Gene: PIK3CA

Linked Data

• dbSNP Id: rs1215652300
• MyVariant Identifiers: chr3:g.178952083A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234295A>T , CM000665.2:g.179234295A>T	GRCh38
NC_000003.11:g.178952083A>T , CM000665.1:g.178952083A>T	GRCh37
NC_000003.10:g.180434777A>T	NCBI36
NG_012113.2:g.90773A>T , LRG_310:g.90773A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3138A>T MANE Select	ENSP00000263967.3:p.Ala1046=
ENST00000462255.2:n.2161A>T
ENST00000643187.1:c.*218A>T	ENSP00000493507.1:n.*218A>T
ENST00000674534.1:n.4046A>T
ENST00000674622.1:c.1559A>T	ENSP00000502417.1:n.1559A>T
ENST00000675467.1:n.5945A>T
ENST00000675786.1:c.*1705A>T	ENSP00000502323.1:n.*1705A>T
ENST00000675796.1:n.3033A>T
ENST00000263967.3:c.3138A>T	ENSP00000263967.3:p.Ala1046=
NM_006218.2:c.3138A>T , LRG_310t1:c.3138A>T	NP_006209.2:p.Ala1046=
XM_006713658.2:c.3138A>T	XP_006713721.1:p.Ala1046=
XM_011512894.1:c.3138A>T	XP_011511196.1:p.Ala1046=
NM_006218.3:c.3138A>T	NP_006209.2:p.Ala1046=
XM_006713658.4:c.3138A>T	XP_006713721.1:p.Ala1046=
XM_011512894.2:c.3138A>T	XP_011511196.1:p.Ala1046=
NM_006218.4:c.3138A>T MANE Select	NP_006209.2:p.Ala1046=