Canonical Allele Identifier: CA355285743
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179234268G>T , CM000665.2:g.179234268G>T GRCh38
NC_000003.11:g.178952056G>T , CM000665.1:g.178952056G>T GRCh37
NC_000003.10:g.180434750G>T NCBI36
NG_012113.2:g.90746G>T , LRG_310:g.90746G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.3111G>T MANE Select ENSP00000263967.3:p.Glu1037Asp
ENST00000462255.2:n.2134G>T
ENST00000643187.1:c.*191G>T ENSP00000493507.1:n.*191G>T
ENST00000674534.1:n.4019G>T
ENST00000674622.1:c.1532G>T ENSP00000502417.1:n.1532G>T
ENST00000675467.1:n.5918G>T
ENST00000675786.1:c.*1678G>T ENSP00000502323.1:n.*1678G>T
ENST00000675796.1:n.3006G>T
ENST00000263967.3:c.3111G>T ENSP00000263967.3:p.Glu1037Asp
NM_006218.2:c.3111G>T , LRG_310t1:c.3111G>T NP_006209.2:p.Glu1037Asp
XM_006713658.2:c.3111G>T XP_006713721.1:p.Glu1037Asp
XM_011512894.1:c.3111G>T XP_011511196.1:p.Glu1037Asp
NM_006218.3:c.3111G>T NP_006209.2:p.Glu1037Asp
XM_006713658.4:c.3111G>T XP_006713721.1:p.Glu1037Asp
XM_011512894.2:c.3111G>T XP_011511196.1:p.Glu1037Asp
NM_006218.4:c.3111G>T MANE Select NP_006209.2:p.Glu1037Asp