Canonical Allele Identifier: CA355285088
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs1725279968

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179234185A>T , CM000665.2:g.179234185A>T GRCh38
NC_000003.11:g.178951973A>T , CM000665.1:g.178951973A>T GRCh37
NC_000003.10:g.180434667A>T NCBI36
NG_012113.2:g.90663A>T , LRG_310:g.90663A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.3028A>T MANE Select ENSP00000263967.3:p.Met1010Leu
ENST00000462255.2:n.2051A>T
ENST00000643187.1:c.*108A>T ENSP00000493507.1:n.*108A>T
ENST00000674534.1:n.3936A>T
ENST00000674622.1:c.1449A>T ENSP00000502417.1:n.1449A>T
ENST00000675467.1:n.5835A>T
ENST00000675786.1:c.*1595A>T ENSP00000502323.1:n.*1595A>T
ENST00000675796.1:n.2923A>T
ENST00000263967.3:c.3028A>T ENSP00000263967.3:p.Met1010Leu
NM_006218.2:c.3028A>T , LRG_310t1:c.3028A>T NP_006209.2:p.Met1010Leu
XM_006713658.2:c.3028A>T XP_006713721.1:p.Met1010Leu
XM_011512894.1:c.3028A>T XP_011511196.1:p.Met1010Leu
NM_006218.3:c.3028A>T NP_006209.2:p.Met1010Leu
XM_006713658.4:c.3028A>T XP_006713721.1:p.Met1010Leu
XM_011512894.2:c.3028A>T XP_011511196.1:p.Met1010Leu
NM_006218.4:c.3028A>T MANE Select NP_006209.2:p.Met1010Leu