Canonical Allele Identifier: CA2668622320
Gene: PIK3CA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179218202T>G , CM000665.2:g.179218202T>G GRCh38
NC_000003.11:g.178935990T>G , CM000665.1:g.178935990T>G GRCh37
NC_000003.10:g.180418684T>G NCBI36
NG_012113.2:g.74680T>G , LRG_310:g.74680T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263967.4:c.1540-8T>G MANE Select ENSP00000263967.3:n.1540-8T>G
ENST00000643187.1:c.1540-8T>G ENSP00000493507.1:n.1540-8T>G
ENST00000674534.1:n.1294-8T>G
ENST00000674622.1:c.43-8T>G ENSP00000502417.1:n.43-8T>G
ENST00000675467.1:n.4347-8T>G
ENST00000675786.1:c.*107-8T>G ENSP00000502323.1:n.*107-8T>G
ENST00000263967.3:c.1540-8T>G ENSP00000263967.3:n.1540-8T>G
NM_006218.2:c.1540-8T>G , LRG_310t1:c.1540-8T>G NP_006209.2:n.1540-8T>G
XM_006713658.2:c.1540-8T>G XP_006713721.1:n.1540-8T>G
XM_011512894.1:c.1540-8T>G XP_011511196.1:n.1540-8T>G
NM_006218.3:c.1540-8T>G NP_006209.2:n.1540-8T>G
XM_006713658.4:c.1540-8T>G XP_006713721.1:n.1540-8T>G
XM_011512894.2:c.1540-8T>G XP_011511196.1:n.1540-8T>G
NM_006218.4:c.1540-8T>G MANE Select NP_006209.2:n.1540-8T>G