Canonical Allele Identifier: CA4429241
Community Standard Title: NM_001282426.2(PIK3CG):c.711del (p.Asp238ThrfsTer21)
Gene: PIK3CG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.106868272del , CM000669.2:g.106868272del GRCh38
NC_000007.13:g.106508717del , CM000669.1:g.106508717del GRCh37
NC_000007.12:g.106295953del NCBI36
NG_050579.1:g.7995del

Transcript Alleles

HGVS Amino-acid Change
NM_001282426.2:c.711del MANE Select NP_001269355.1:p.Asp238ThrfsTer21
ENST00000496166.6:c.711del MANE Select ENSP00000419260.1:p.Asp238ThrfsTer21
NM_001282426.1:c.711del NP_001269355.1:p.Asp238ThrfsTer21
NM_001282427.1:c.711del NP_001269356.1:p.Asp238ThrfsTer21
NM_001282427.2:c.711del NP_001269356.1:p.Asp238ThrfsTer21
NM_002649.3:c.711del NP_002640.2:p.Asp238ThrfsTer21
ENST00000359195.3:c.711del ENSP00000352121.3:p.Asp238ThrfsTer21
ENST00000440650.6:c.711del ENSP00000392258.2:p.Asp238ThrfsTer21
ENST00000473541.5:c.-187+2846del ENSP00000417623.1:n.-187+2846del
ENST00000496166.5:c.711del ENSP00000419260.1:p.Asp238ThrfsTer21
XM_005250443.2:c.711del XP_005250500.1:p.Asp238ThrfsTer21
XM_005250443.3:c.711del XP_005250500.1:p.Asp238ThrfsTer21
XM_011516316.1:c.711del XP_011514618.1:p.Asp238ThrfsTer21
XM_011516317.1:c.711del XP_011514619.1:p.Asp238ThrfsTer21
XM_017012328.1:c.711del XP_016867817.1:p.Asp238ThrfsTer21