Canonical Allele Identifier: CA2710592
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs773463783

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179203511C>A , CM000665.2:g.179203511C>A GRCh38
NC_000003.11:g.178921299C>A , CM000665.1:g.178921299C>A GRCh37
NC_000003.10:g.180403993C>A NCBI36
NG_012113.2:g.59989C>A , LRG_310:g.59989C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.814-33C>A MANE Select ENSP00000263967.3:n.814-33C>A
ENST00000643187.1:c.814-33C>A ENSP00000493507.1:n.814-33C>A
ENST00000674534.1:n.535C>A
ENST00000675467.1:n.3621-33C>A
ENST00000675786.1:c.814-33C>A ENSP00000502323.1:n.814-33C>A
ENST00000263967.3:c.814-33C>A ENSP00000263967.3:n.814-33C>A
NM_006218.2:c.814-33C>A , LRG_310t1:c.814-33C>A NP_006209.2:n.814-33C>A
XM_006713658.2:c.814-33C>A XP_006713721.1:n.814-33C>A
XM_011512894.1:c.814-33C>A XP_011511196.1:n.814-33C>A
NM_006218.3:c.814-33C>A NP_006209.2:n.814-33C>A
XM_006713658.4:c.814-33C>A XP_006713721.1:n.814-33C>A
XM_011512894.2:c.814-33C>A XP_011511196.1:n.814-33C>A
NM_006218.4:c.814-33C>A MANE Select NP_006209.2:n.814-33C>A