Canonical Allele Identifier: CA1423660551
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs1724236815

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179195225C>A , CM000665.2:g.179195225C>A GRCh38
NC_000003.11:g.178913013C>A , CM000665.1:g.178913013C>A GRCh37
NC_000003.10:g.180395707C>A NCBI36
NG_012113.2:g.51703C>A , LRG_310:g.51703C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.-76-3525C>A MANE Select ENSP00000263967.3:n.-76-3525C>A
ENST00000643187.1:c.-76-3525C>A ENSP00000493507.1:n.-76-3525C>A
ENST00000675786.1:c.-76-3525C>A ENSP00000502323.1:n.-76-3525C>A
ENST00000263967.3:c.-76-3525C>A ENSP00000263967.3:n.-76-3525C>A
ENST00000468036.1:c.-76-3525C>A ENSP00000417479.1:n.-76-3525C>A
ENST00000477735.1:c.-76-3525C>A ENSP00000418145.1:n.-76-3525C>A
NM_006218.2:c.-76-3525C>A , LRG_310t1:c.-76-3525C>A NP_006209.2:n.-76-3525C>A
XM_006713658.2:c.-76-3525C>A XP_006713721.1:n.-76-3525C>A
XM_011512894.1:c.-76-3525C>A XP_011511196.1:n.-76-3525C>A
NM_006218.3:c.-76-3525C>A NP_006209.2:n.-76-3525C>A
XM_006713658.4:c.-76-3525C>A XP_006713721.1:n.-76-3525C>A
XM_011512894.2:c.-76-3525C>A XP_011511196.1:n.-76-3525C>A
NM_006218.4:c.-76-3525C>A MANE Select NP_006209.2:n.-76-3525C>A