Canonical Allele Identifier: CA437032864
Gene: PIK3CA HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.178936006A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218218A>G , CM000665.2:g.179218218A>G GRCh38
NC_000003.11:g.178936006A>G , CM000665.1:g.178936006A>G GRCh37
NC_000003.10:g.180418700A>G NCBI36
NG_012113.2:g.74696A>G , LRG_310:g.74696A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1548A>G MANE Select ENSP00000263967.3:p.Arg516=
ENST00000462255.2:n.10A>G
ENST00000643187.1:c.1548A>G ENSP00000493507.1:p.Arg516=
ENST00000674534.1:n.1302A>G
ENST00000674622.1:c.51A>G ENSP00000502417.1:p.Arg17=
ENST00000675467.1:n.4355A>G
ENST00000675786.1:c.*115A>G ENSP00000502323.1:n.*115A>G
ENST00000263967.3:c.1548A>G ENSP00000263967.3:p.Arg516=
NM_006218.2:c.1548A>G , LRG_310t1:c.1548A>G NP_006209.2:p.Arg516=
XM_006713658.2:c.1548A>G XP_006713721.1:p.Arg516=
XM_011512894.1:c.1548A>G XP_011511196.1:p.Arg516=
NM_006218.3:c.1548A>G NP_006209.2:p.Arg516=
XM_006713658.4:c.1548A>G XP_006713721.1:p.Arg516=
XM_011512894.2:c.1548A>G XP_011511196.1:p.Arg516=
NM_006218.4:c.1548A>G MANE Select NP_006209.2:p.Arg516=