Canonical Allele Identifier: CA338301102
Community Standard Title: NM_005026.5(PIK3CD):c.658G>T (p.Ala220Ser)
Gene: PIK3CD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9716497G>T , CM000663.2:g.9716497G>T GRCh38
NC_000001.10:g.9776555G>T , CM000663.1:g.9776555G>T GRCh37
NC_000001.9:g.9699142G>T NCBI36
NG_023434.1:g.69766G>T , LRG_191:g.69766G>T

Transcript Alleles

HGVS Amino-acid Change
NM_005026.5:c.658G>T MANE Select NP_005017.3:p.Ala220Ser
ENST00000377346.9:c.658G>T MANE Select ENSP00000366563.4:p.Ala220Ser
NM_001350234.1:c.658G>T NP_001337163.1:p.Ala220Ser
NM_001350234.2:c.658G>T NP_001337163.1:p.Ala220Ser
NM_001350235.1:c.658G>T NP_001337164.1:p.Ala220Ser
NM_005026.3:c.658G>T , LRG_191t1:c.658G>T NP_005017.3:p.Ala220Ser
NM_005026.4:c.658G>T NP_005017.3:p.Ala220Ser
ENST00000361110.6:c.658G>T ENSP00000354410.2:p.Ala220Ser
ENST00000377346.8:c.658G>T ENSP00000366563.4:p.Ala220Ser
ENST00000479223.1:n.222G>T
ENST00000481137.2:c.821G>T ENSP00000513886.1:p.Cys274Phe
ENST00000536656.5:c.658G>T ENSP00000446444.2:p.Ala220Ser
ENST00000543390.2:c.658G>T ENSP00000443811.2:p.Ala220Ser
ENST00000628140.2:c.658G>T ENSP00000486826.1:p.Ala220Ser
ENST00000698709.1:c.658G>T ENSP00000513887.1:p.Ala220Ser
ENST00000698710.1:c.658G>T ENSP00000513888.1:p.Ala220Ser
ENST00000698711.1:n.1372G>T
ENST00000698712.1:c.658G>T ENSP00000513889.1:p.Ala220Ser
ENST00000698713.1:c.658G>T ENSP00000513890.1:p.Ala220Ser
ENST00000698714.1:c.658G>T ENSP00000513891.1:p.Ala220Ser
ENST00000698715.1:c.658G>T ENSP00000513892.1:p.Ala220Ser
ENST00000698716.1:c.658G>T ENSP00000513893.1:p.Ala220Ser
ENST00000698717.1:n.657G>T
XM_005263473.1:c.658G>T XP_005263530.1:p.Ala220Ser
XM_006710686.1:c.658G>T XP_006710749.1:p.Ala220Ser
XM_006710687.1:c.658G>T XP_006710750.1:p.Ala220Ser
XM_006710687.2:c.658G>T XP_006710750.1:p.Ala220Ser
XM_006710688.1:c.658G>T XP_006710751.1:p.Ala220Ser
XM_006710689.1:c.658G>T XP_006710752.1:p.Ala220Ser
XM_006710689.2:c.658G>T XP_006710752.1:p.Ala220Ser
XM_006710690.1:c.658G>T XP_006710753.1:p.Ala220Ser
XM_011541581.1:c.658G>T XP_011539883.1:p.Ala220Ser
XM_011541582.1:c.658G>T XP_011539884.1:p.Ala220Ser
XM_011541583.1:c.10G>T XP_011539885.1:p.Ala4Ser
XM_017001476.1:c.658G>T XP_016856965.1:p.Ala220Ser
XM_017001477.1:c.658G>T XP_016856966.1:p.Ala220Ser
XM_017001478.1:c.658G>T XP_016856967.1:p.Ala220Ser
XM_017001479.1:c.658G>T XP_016856968.1:p.Ala220Ser
XM_017001480.1:c.658G>T XP_016856969.1:p.Ala220Ser
XM_017001481.1:c.658G>T XP_016856970.1:p.Ala220Ser
XM_017001482.2:c.658G>T XP_016856971.1:p.Ala220Ser
XM_017001483.2:c.658G>T XP_016856972.1:p.Ala220Ser
XM_024447661.1:c.658G>T XP_024303429.1:p.Ala220Ser
XM_024447663.1:c.658G>T XP_024303431.1:p.Ala220Ser
XM_024447664.1:c.658G>T XP_024303432.1:p.Ala220Ser
XR_002956806.1:n.867G>T
XR_946667.1:n.867G>T