Canonical Allele Identifier: CA355279691
Community Standard Title: NM_006218.4(PIK3CA):c.2727C>G (p.Phe909Leu)
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179230064C>G , CM000665.2:g.179230064C>G GRCh38
NC_000003.11:g.178947852C>G , CM000665.1:g.178947852C>G GRCh37
NC_000003.10:g.180430546C>G NCBI36
NG_012113.2:g.86542C>G , LRG_310:g.86542C>G

Transcript Alleles

HGVS Amino-acid Change
NM_006218.4:c.2727C>G MANE Select NP_006209.2:p.Phe909Leu
ENST00000263967.4:c.2727C>G MANE Select ENSP00000263967.3:p.Phe909Leu
NM_006218.2:c.2727C>G , LRG_310t1:c.2727C>G NP_006209.2:p.Phe909Leu
NM_006218.3:c.2727C>G NP_006209.2:p.Phe909Leu
ENST00000263967.3:c.2727C>G ENSP00000263967.3:p.Phe909Leu
ENST00000462255.2:n.1750C>G
ENST00000643187.1:c.2727C>G ENSP00000493507.1:p.Phe909Leu
ENST00000674534.1:n.3635C>G
ENST00000674622.1:c.1148C>G ENSP00000502417.1:n.1148C>G
ENST00000675467.1:n.5534C>G
ENST00000675786.1:c.*1294C>G ENSP00000502323.1:n.*1294C>G
ENST00000675796.1:n.2622C>G
XM_006713658.2:c.2727C>G XP_006713721.1:p.Phe909Leu
XM_006713658.4:c.2727C>G XP_006713721.1:p.Phe909Leu
XM_011512894.1:c.2727C>G XP_011511196.1:p.Phe909Leu
XM_011512894.2:c.2727C>G XP_011511196.1:p.Phe909Leu