Canonical Allele Identifier: CA2668621545
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179210138A>T , CM000665.2:g.179210138A>T GRCh38
NC_000003.11:g.178927926A>T , CM000665.1:g.178927926A>T GRCh37
NC_000003.10:g.180410620A>T NCBI36
NG_012113.2:g.66616A>T , LRG_310:g.66616A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1252-48A>T MANE Select ENSP00000263967.3:n.1252-48A>T
ENST00000643187.1:c.1252-48A>T ENSP00000493507.1:n.1252-48A>T
ENST00000674534.1:n.1006-48A>T
ENST00000675467.1:n.4059-48A>T
ENST00000675786.1:c.1252-48A>T ENSP00000502323.1:n.1252-48A>T
ENST00000263967.3:c.1252-48A>T ENSP00000263967.3:n.1252-48A>T
NM_006218.2:c.1252-48A>T , LRG_310t1:c.1252-48A>T NP_006209.2:n.1252-48A>T
XM_006713658.2:c.1252-48A>T XP_006713721.1:n.1252-48A>T
XM_011512894.1:c.1252-48A>T XP_011511196.1:n.1252-48A>T
NM_006218.3:c.1252-48A>T NP_006209.2:n.1252-48A>T
XM_006713658.4:c.1252-48A>T XP_006713721.1:n.1252-48A>T
XM_011512894.2:c.1252-48A>T XP_011511196.1:n.1252-48A>T
NM_006218.4:c.1252-48A>T MANE Select NP_006209.2:n.1252-48A>T