Canonical Allele Identifier: CA1423672809
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs1724799817

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179214780G>A , CM000665.2:g.179214780G>A GRCh38
NC_000003.11:g.178932568G>A , CM000665.1:g.178932568G>A GRCh37
NC_000003.10:g.180415262G>A NCBI36
NG_012113.2:g.71258G>A , LRG_310:g.71258G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.1540-3430G>A MANE Select ENSP00000263967.3:n.1540-3430G>A
ENST00000643187.1:c.1540-3430G>A ENSP00000493507.1:n.1540-3430G>A
ENST00000674534.1:n.1294-3430G>A
ENST00000674622.1:c.43-3430G>A ENSP00000502417.1:n.43-3430G>A
ENST00000675467.1:n.4347-3430G>A
ENST00000675786.1:c.*107-3430G>A ENSP00000502323.1:n.*107-3430G>A
ENST00000263967.3:c.1540-3430G>A ENSP00000263967.3:n.1540-3430G>A
NM_006218.2:c.1540-3430G>A , LRG_310t1:c.1540-3430G>A NP_006209.2:n.1540-3430G>A
XM_006713658.2:c.1540-3430G>A XP_006713721.1:n.1540-3430G>A
XM_011512894.1:c.1540-3430G>A XP_011511196.1:n.1540-3430G>A
NM_006218.3:c.1540-3430G>A NP_006209.2:n.1540-3430G>A
XM_006713658.4:c.1540-3430G>A XP_006713721.1:n.1540-3430G>A
XM_011512894.2:c.1540-3430G>A XP_011511196.1:n.1540-3430G>A
NM_006218.4:c.1540-3430G>A MANE Select NP_006209.2:n.1540-3430G>A