Canonical Allele Identifier: CA2668622507
Gene: PIK3CA HGNC NCBI

Linked Data

dbSNP Id: rs2108408657

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218391T>A , CM000665.2:g.179218391T>A GRCh38
NC_000003.11:g.178936179T>A , CM000665.1:g.178936179T>A GRCh37
NC_000003.10:g.180418873T>A NCBI36
NG_012113.2:g.74869T>A , LRG_310:g.74869T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1664+57T>A MANE Select ENSP00000263967.3:n.1664+57T>A
ENST00000462255.2:n.126+57T>A
ENST00000643187.1:c.1664+57T>A ENSP00000493507.1:n.1664+57T>A
ENST00000674534.1:n.1475T>A
ENST00000674622.1:c.167+57T>A ENSP00000502417.1:n.167+57T>A
ENST00000675467.1:n.4471+57T>A
ENST00000675786.1:c.*231+57T>A ENSP00000502323.1:n.*231+57T>A
ENST00000263967.3:c.1664+57T>A ENSP00000263967.3:n.1664+57T>A
NM_006218.2:c.1664+57T>A , LRG_310t1:c.1664+57T>A NP_006209.2:n.1664+57T>A
XM_006713658.2:c.1664+57T>A XP_006713721.1:n.1664+57T>A
XM_011512894.1:c.1664+57T>A XP_011511196.1:n.1664+57T>A
NM_006218.3:c.1664+57T>A NP_006209.2:n.1664+57T>A
XM_006713658.4:c.1664+57T>A XP_006713721.1:n.1664+57T>A
XM_011512894.2:c.1664+57T>A XP_011511196.1:n.1664+57T>A
NM_006218.4:c.1664+57T>A MANE Select NP_006209.2:n.1664+57T>A