Canonical Allele Identifier: CA355285257
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108429427

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179234201C>G , CM000665.2:g.179234201C>G GRCh38
NC_000003.11:g.178951989C>G , CM000665.1:g.178951989C>G GRCh37
NC_000003.10:g.180434683C>G NCBI36
NG_012113.2:g.90679C>G , LRG_310:g.90679C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.3044C>G MANE Select ENSP00000263967.3:p.Ser1015Cys
ENST00000462255.2:n.2067C>G
ENST00000643187.1:c.*124C>G ENSP00000493507.1:n.*124C>G
ENST00000674534.1:n.3952C>G
ENST00000674622.1:c.1465C>G ENSP00000502417.1:n.1465C>G
ENST00000675467.1:n.5851C>G
ENST00000675786.1:c.*1611C>G ENSP00000502323.1:n.*1611C>G
ENST00000675796.1:n.2939C>G
ENST00000263967.3:c.3044C>G ENSP00000263967.3:p.Ser1015Cys
NM_006218.2:c.3044C>G , LRG_310t1:c.3044C>G NP_006209.2:p.Ser1015Cys
XM_006713658.2:c.3044C>G XP_006713721.1:p.Ser1015Cys
XM_011512894.1:c.3044C>G XP_011511196.1:p.Ser1015Cys
NM_006218.3:c.3044C>G NP_006209.2:p.Ser1015Cys
XM_006713658.4:c.3044C>G XP_006713721.1:p.Ser1015Cys
XM_011512894.2:c.3044C>G XP_011511196.1:p.Ser1015Cys
NM_006218.4:c.3044C>G MANE Select NP_006209.2:p.Ser1015Cys