Canonical Allele Identifier: CA355264830
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108408128

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218259A>T , CM000665.2:g.179218259A>T GRCh38
NC_000003.11:g.178936047A>T , CM000665.1:g.178936047A>T GRCh37
NC_000003.10:g.180418741A>T NCBI36
NG_012113.2:g.74737A>T , LRG_310:g.74737A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1589A>T MANE Select ENSP00000263967.3:p.Gln530Leu
ENST00000462255.2:n.51A>T
ENST00000643187.1:c.1589A>T ENSP00000493507.1:p.Gln530Leu
ENST00000674534.1:n.1343A>T
ENST00000674622.1:c.92A>T ENSP00000502417.1:p.Gln31Leu
ENST00000675467.1:n.4396A>T
ENST00000675786.1:c.*156A>T ENSP00000502323.1:n.*156A>T
ENST00000263967.3:c.1589A>T ENSP00000263967.3:p.Gln530Leu
NM_006218.2:c.1589A>T , LRG_310t1:c.1589A>T NP_006209.2:p.Gln530Leu
XM_006713658.2:c.1589A>T XP_006713721.1:p.Gln530Leu
XM_011512894.1:c.1589A>T XP_011511196.1:p.Gln530Leu
NM_006218.3:c.1589A>T NP_006209.2:p.Gln530Leu
XM_006713658.4:c.1589A>T XP_006713721.1:p.Gln530Leu
XM_011512894.2:c.1589A>T XP_011511196.1:p.Gln530Leu
NM_006218.4:c.1589A>T MANE Select NP_006209.2:p.Gln530Leu