Canonical Allele Identifier: CA1423660518
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs870995

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179195218C>G , CM000665.2:g.179195218C>G GRCh38
NC_000003.11:g.178913006C>G , CM000665.1:g.178913006C>G GRCh37
NC_000003.10:g.180395700C>G NCBI36
NG_012113.2:g.51696C>G , LRG_310:g.51696C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.-76-3532C>G MANE Select ENSP00000263967.3:n.-76-3532C>G
ENST00000643187.1:c.-76-3532C>G ENSP00000493507.1:n.-76-3532C>G
ENST00000675786.1:c.-76-3532C>G ENSP00000502323.1:n.-76-3532C>G
ENST00000263967.3:c.-76-3532C>G ENSP00000263967.3:n.-76-3532C>G
ENST00000468036.1:c.-76-3532C>G ENSP00000417479.1:n.-76-3532C>G
ENST00000477735.1:c.-76-3532C>G ENSP00000418145.1:n.-76-3532C>G
NM_006218.2:c.-76-3532C>G , LRG_310t1:c.-76-3532C>G NP_006209.2:n.-76-3532C>G
XM_006713658.2:c.-76-3532C>G XP_006713721.1:n.-76-3532C>G
XM_011512894.1:c.-76-3532C>G XP_011511196.1:n.-76-3532C>G
NM_006218.3:c.-76-3532C>G NP_006209.2:n.-76-3532C>G
XM_006713658.4:c.-76-3532C>G XP_006713721.1:n.-76-3532C>G
XM_011512894.2:c.-76-3532C>G XP_011511196.1:n.-76-3532C>G
NM_006218.4:c.-76-3532C>G MANE Select NP_006209.2:n.-76-3532C>G