Canonical Allele Identifier: CA2577963296
Gene: PIK3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179210145_179210146del , CM000665.2:g.179210145_179210146del GRCh38
NC_000003.11:g.178927933_178927934del , CM000665.1:g.178927933_178927934del GRCh37
NC_000003.10:g.180410627_180410628del NCBI36
NG_012113.2:g.66623_66624del , LRG_310:g.66623_66624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263967.4:c.1252-41_1252-40del MANE Select ENSP00000263967.3:n.1252-41_1252-40del
ENST00000643187.1:c.1252-41_1252-40del ENSP00000493507.1:n.1252-41_1252-40del
ENST00000674534.1:n.1006-41_1006-40del
ENST00000675467.1:n.4059-41_4059-40del
ENST00000675786.1:c.1252-41_1252-40del ENSP00000502323.1:n.1252-41_1252-40del
ENST00000263967.3:c.1252-41_1252-40del ENSP00000263967.3:n.1252-41_1252-40del
NM_006218.2:c.1252-41_1252-40del , LRG_310t1:c.1252-41_1252-40del NP_006209.2:n.1252-41_1252-40del
XM_006713658.2:c.1252-41_1252-40del XP_006713721.1:n.1252-41_1252-40del
XM_011512894.1:c.1252-41_1252-40del XP_011511196.1:n.1252-41_1252-40del
NM_006218.3:c.1252-41_1252-40del NP_006209.2:n.1252-41_1252-40del
XM_006713658.4:c.1252-41_1252-40del XP_006713721.1:n.1252-41_1252-40del
XM_011512894.2:c.1252-41_1252-40del XP_011511196.1:n.1252-41_1252-40del
NM_006218.4:c.1252-41_1252-40del MANE Select NP_006209.2:n.1252-41_1252-40del