Canonical Allele Identifier: CA355270947
Community Standard Title: NM_006218.4(PIK3CA):c.2275C>T (p.His759Tyr)
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179224168C>T , CM000665.2:g.179224168C>T GRCh38
NC_000003.11:g.178941956C>T , CM000665.1:g.178941956C>T GRCh37
NC_000003.10:g.180424650C>T NCBI36
NG_012113.2:g.80646C>T , LRG_310:g.80646C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006218.4:c.2275C>T MANE Select NP_006209.2:p.His759Tyr
ENST00000263967.4:c.2275C>T MANE Select ENSP00000263967.3:p.His759Tyr
NM_006218.2:c.2275C>T , LRG_310t1:c.2275C>T NP_006209.2:p.His759Tyr
NM_006218.3:c.2275C>T NP_006209.2:p.His759Tyr
ENST00000263967.3:c.2275C>T ENSP00000263967.3:p.His759Tyr
ENST00000462255.1:n.549C>T
ENST00000462255.2:n.737C>T
ENST00000643187.1:c.2275C>T ENSP00000493507.1:p.His759Tyr
ENST00000674534.1:n.3183C>T
ENST00000674622.1:c.696C>T ENSP00000502417.1:n.696C>T
ENST00000675467.1:n.5082C>T
ENST00000675786.1:c.*842C>T ENSP00000502323.1:n.*842C>T
XM_006713658.2:c.2275C>T XP_006713721.1:p.His759Tyr
XM_006713658.4:c.2275C>T XP_006713721.1:p.His759Tyr
XM_011512894.1:c.2275C>T XP_011511196.1:p.His759Tyr
XM_011512894.2:c.2275C>T XP_011511196.1:p.His759Tyr