Canonical Allele Identifier: CA355285711

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234261C>T , CM000665.2:g.179234261C>T	GRCh38
NC_000003.11:g.178952049C>T , CM000665.1:g.178952049C>T	GRCh37
NC_000003.10:g.180434743C>T	NCBI36
NG_012113.2:g.90739C>T , LRG_310:g.90739C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006218.4:c.3104C>T MANE Select	NP_006209.2:p.Ala1035Val
ENST00000263967.4:c.3104C>T MANE Select	ENSP00000263967.3:p.Ala1035Val
NM_006218.2:c.3104C>T , LRG_310t1:c.3104C>T	NP_006209.2:p.Ala1035Val
NM_006218.3:c.3104C>T	NP_006209.2:p.Ala1035Val
ENST00000263967.3:c.3104C>T	ENSP00000263967.3:p.Ala1035Val
ENST00000462255.2:n.2127C>T
ENST00000643187.1:c.*184C>T	ENSP00000493507.1:n.*184C>T
ENST00000674534.1:n.4012C>T
ENST00000674622.1:c.1525C>T	ENSP00000502417.1:n.1525C>T
ENST00000675467.1:n.5911C>T
ENST00000675786.1:c.*1671C>T	ENSP00000502323.1:n.*1671C>T
ENST00000675796.1:n.2999C>T
XM_006713658.2:c.3104C>T	XP_006713721.1:p.Ala1035Val
XM_006713658.4:c.3104C>T	XP_006713721.1:p.Ala1035Val
XM_011512894.1:c.3104C>T	XP_011511196.1:p.Ala1035Val
XM_011512894.2:c.3104C>T	XP_011511196.1:p.Ala1035Val