Canonical Allele Identifier: CA4429401
Gene: PIK3CG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.106869174C>T , CM000669.2:g.106869174C>T GRCh38
NC_000007.13:g.106509619C>T , CM000669.1:g.106509619C>T GRCh37
NC_000007.12:g.106296855C>T NCBI36
NG_050579.1:g.8897C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496166.6:c.1613C>T MANE Select ENSP00000419260.1:p.Pro538Leu
ENST00000359195.3:c.1613C>T ENSP00000352121.3:p.Pro538Leu
ENST00000440650.6:c.1613C>T ENSP00000392258.2:p.Pro538Leu
ENST00000473541.5:c.-186-3363C>T ENSP00000417623.1:n.-186-3363C>T
ENST00000496166.5:c.1613C>T ENSP00000419260.1:p.Pro538Leu
NM_001282426.1:c.1613C>T NP_001269355.1:p.Pro538Leu
NM_001282427.1:c.1613C>T NP_001269356.1:p.Pro538Leu
NM_002649.3:c.1613C>T NP_002640.2:p.Pro538Leu
XM_005250443.2:c.1613C>T XP_005250500.1:p.Pro538Leu
XM_011516316.1:c.1613C>T XP_011514618.1:p.Pro538Leu
XM_011516317.1:c.1613C>T XP_011514619.1:p.Pro538Leu
XM_005250443.3:c.1613C>T XP_005250500.1:p.Pro538Leu
XM_017012328.1:c.1613C>T XP_016867817.1:p.Pro538Leu
NM_001282426.2:c.1613C>T MANE Select NP_001269355.1:p.Pro538Leu
NM_001282427.2:c.1613C>T NP_001269356.1:p.Pro538Leu