Canonical Allele Identifier: CA2704642319

Gene: PIK3CA

Linked Data

• dbSNP Id: rs2108430250

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234385A>T , CM000665.2:g.179234385A>T	GRCh38
NC_000003.11:g.178952173A>T , CM000665.1:g.178952173A>T	GRCh37
NC_000003.10:g.180434867A>T	NCBI36
NG_012113.2:g.90863A>T , LRG_310:g.90863A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.*21A>T MANE Select	ENSP00000263967.3:n.*21A>T
ENST00000462255.2:n.2251A>T
ENST00000643187.1:c.*308A>T	ENSP00000493507.1:n.*308A>T
ENST00000674534.1:n.4136A>T
ENST00000674622.1:c.1649A>T	ENSP00000502417.1:n.1649A>T
ENST00000675467.1:n.6035A>T
ENST00000675786.1:c.*1795A>T	ENSP00000502323.1:n.*1795A>T
ENST00000675796.1:n.3123A>T
ENST00000263967.3:c.*21A>T	ENSP00000263967.3:n.*21A>T
NM_006218.2:c.*21A>T , LRG_310t1:c.*21A>T	NP_006209.2:n.*21A>T
XM_006713658.2:c.*21A>T	XP_006713721.1:n.*21A>T
XM_011512894.1:c.*21A>T	XP_011511196.1:n.*21A>T
NM_006218.3:c.*21A>T	NP_006209.2:n.*21A>T
XM_006713658.4:c.*21A>T	XP_006713721.1:n.*21A>T
XM_011512894.2:c.*21A>T	XP_011511196.1:n.*21A>T
NM_006218.4:c.*21A>T MANE Select	NP_006209.2:n.*21A>T