Canonical Allele Identifier: CA1423674623
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179219495A= , CM000665.2:g.179219495A= GRCh38
NC_000003.11:g.178937283A= , CM000665.1:g.178937283A= GRCh37
NC_000003.10:g.180419977A= NCBI36
NG_012113.2:g.75973A= , LRG_310:g.75973A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1747-76A= MANE Select ENSP00000263967.3:n.1747-76A=
ENST00000462255.2:n.209-76A=
ENST00000643187.1:c.1747-76A= ENSP00000493507.1:n.1747-76A=
ENST00000674534.1:n.2579A=
ENST00000674622.1:c.168-76A= ENSP00000502417.1:n.168-76A=
ENST00000675467.1:n.4554-76A=
ENST00000675786.1:c.*314-76A= ENSP00000502323.1:n.*314-76A=
ENST00000263967.3:c.1747-76A= ENSP00000263967.3:n.1747-76A=
NM_006218.2:c.1747-76A= , LRG_310t1:c.1747-76A= NP_006209.2:n.1747-76A=
XM_006713658.2:c.1747-76A= XP_006713721.1:n.1747-76A=
XM_011512894.1:c.1747-76A= XP_011511196.1:n.1747-76A=
NM_006218.3:c.1747-76A= NP_006209.2:n.1747-76A=
XM_006713658.4:c.1747-76A= XP_006713721.1:n.1747-76A=
XM_011512894.2:c.1747-76A= XP_011511196.1:n.1747-76A=
NM_006218.4:c.1747-76A= MANE Select NP_006209.2:n.1747-76A=