Canonical Allele Identifier: CA2525589768
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179198729T>C , CM000665.2:g.179198729T>C GRCh38
NC_000003.11:g.178916517T>C , CM000665.1:g.178916517T>C GRCh37
NC_000003.10:g.180399211T>C NCBI36
NG_012113.2:g.55207T>C , LRG_310:g.55207T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.-76-21T>C MANE Select ENSP00000263967.3:n.-76-21T>C
ENST00000643187.1:c.-76-21T>C ENSP00000493507.1:n.-76-21T>C
ENST00000675467.1:n.2711T>C
ENST00000675786.1:c.-76-21T>C ENSP00000502323.1:n.-76-21T>C
ENST00000263967.3:c.-76-21T>C ENSP00000263967.3:n.-76-21T>C
ENST00000468036.1:c.-76-21T>C ENSP00000417479.1:n.-76-21T>C
ENST00000477735.1:c.-76-21T>C ENSP00000418145.1:n.-76-21T>C
NM_006218.2:c.-76-21T>C , LRG_310t1:c.-76-21T>C NP_006209.2:n.-76-21T>C
XM_006713658.2:c.-76-21T>C XP_006713721.1:n.-76-21T>C
XM_011512894.1:c.-76-21T>C XP_011511196.1:n.-76-21T>C
NM_006218.3:c.-76-21T>C NP_006209.2:n.-76-21T>C
XM_006713658.4:c.-76-21T>C XP_006713721.1:n.-76-21T>C
XM_011512894.2:c.-76-21T>C XP_011511196.1:n.-76-21T>C
NM_006218.4:c.-76-21T>C MANE Select NP_006209.2:n.-76-21T>C