Canonical Allele Identifier: CA368827466

Gene: PIK3CG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.106868868G>A , CM000669.2:g.106868868G>A	GRCh38
NC_000007.13:g.106509313G>A , CM000669.1:g.106509313G>A	GRCh37
NC_000007.12:g.106296549G>A	NCBI36
NG_050579.1:g.8591G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496166.6:c.1307G>A MANE Select	ENSP00000419260.1:p.Gly436Asp
ENST00000359195.3:c.1307G>A	ENSP00000352121.3:p.Gly436Asp
ENST00000440650.6:c.1307G>A	ENSP00000392258.2:p.Gly436Asp
ENST00000473541.5:c.-187+3442G>A	ENSP00000417623.1:n.-187+3442G>A
ENST00000496166.5:c.1307G>A	ENSP00000419260.1:p.Gly436Asp
NM_001282426.1:c.1307G>A	NP_001269355.1:p.Gly436Asp
NM_001282427.1:c.1307G>A	NP_001269356.1:p.Gly436Asp
NM_002649.3:c.1307G>A	NP_002640.2:p.Gly436Asp
XM_005250443.2:c.1307G>A	XP_005250500.1:p.Gly436Asp
XM_011516316.1:c.1307G>A	XP_011514618.1:p.Gly436Asp
XM_011516317.1:c.1307G>A	XP_011514619.1:p.Gly436Asp
XM_005250443.3:c.1307G>A	XP_005250500.1:p.Gly436Asp
XM_017012328.1:c.1307G>A	XP_016867817.1:p.Gly436Asp
NM_001282426.2:c.1307G>A MANE Select	NP_001269355.1:p.Gly436Asp
NM_001282427.2:c.1307G>A	NP_001269356.1:p.Gly436Asp