Canonical Allele Identifier: CA577276
Community Standard Title: NM_005026.5(PIK3CD):c.1642C>T (p.Arg548Trp)
Gene: PIK3CD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9720862C>T , CM000663.2:g.9720862C>T GRCh38
NC_000001.10:g.9780920C>T , CM000663.1:g.9780920C>T GRCh37
NC_000001.9:g.9703507C>T NCBI36
NG_023434.1:g.74131C>T , LRG_191:g.74131C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005026.5:c.1642C>T MANE Select NP_005017.3:p.Arg548Trp
ENST00000377346.9:c.1642C>T MANE Select ENSP00000366563.4:p.Arg548Trp
NM_001350234.1:c.1639C>T NP_001337163.1:p.Arg547Trp
NM_001350234.2:c.1639C>T NP_001337163.1:p.Arg547Trp
NM_001350235.1:c.1555C>T NP_001337164.1:p.Arg519Trp
NM_005026.3:c.1642C>T , LRG_191t1:c.1642C>T NP_005017.3:p.Arg548Trp
NM_005026.4:c.1642C>T NP_005017.3:p.Arg548Trp
ENST00000361110.6:c.1714C>T ENSP00000354410.2:p.Arg572Trp
ENST00000377346.8:c.1642C>T ENSP00000366563.4:p.Arg548Trp
ENST00000481137.2:c.*896C>T ENSP00000513886.1:n.*896C>T
ENST00000536656.5:c.1714C>T ENSP00000446444.2:p.Arg572Trp
ENST00000543390.2:c.1714C>T ENSP00000443811.2:p.Arg572Trp
ENST00000628140.2:c.1714C>T ENSP00000486826.1:p.Arg572Trp
ENST00000698709.1:c.1642C>T ENSP00000513887.1:p.Arg548Trp
ENST00000698710.1:c.1639C>T ENSP00000513888.1:p.Arg547Trp
ENST00000698712.1:c.1642C>T ENSP00000513889.1:p.Arg548Trp
ENST00000698713.1:c.1642C>T ENSP00000513890.1:p.Arg548Trp
ENST00000698714.1:c.1642C>T ENSP00000513891.1:p.Arg548Trp
ENST00000698715.1:c.1639C>T ENSP00000513892.1:p.Arg547Trp
ENST00000698716.1:c.1630C>T ENSP00000513893.1:p.Arg544Trp
ENST00000698718.1:n.712C>T
ENST00000698788.1:n.471C>T
ENST00000698789.1:c.318C>T
XM_005263473.1:c.1639C>T XP_005263530.1:p.Arg547Trp
XM_006710686.1:c.1642C>T XP_006710749.1:p.Arg548Trp
XM_006710687.1:c.1642C>T XP_006710750.1:p.Arg548Trp
XM_006710687.2:c.1642C>T XP_006710750.1:p.Arg548Trp
XM_006710688.1:c.1642C>T XP_006710751.1:p.Arg548Trp
XM_006710689.1:c.1642C>T XP_006710752.1:p.Arg548Trp
XM_006710689.2:c.1642C>T XP_006710752.1:p.Arg548Trp
XM_006710690.1:c.1555C>T XP_006710753.1:p.Arg519Trp
XM_011541581.1:c.1642C>T XP_011539883.1:p.Arg548Trp
XM_011541582.1:c.1642C>T XP_011539884.1:p.Arg548Trp
XM_011541583.1:c.994C>T XP_011539885.1:p.Arg332Trp
XM_017001476.1:c.1819C>T XP_016856965.1:p.Arg607Trp
XM_017001477.1:c.1819C>T XP_016856966.1:p.Arg607Trp
XM_017001478.1:c.1819C>T XP_016856967.1:p.Arg607Trp
XM_017001479.1:c.1819C>T XP_016856968.1:p.Arg607Trp
XM_017001480.1:c.1819C>T XP_016856969.1:p.Arg607Trp
XM_017001481.1:c.1819C>T XP_016856970.1:p.Arg607Trp
XM_017001482.2:c.1819C>T XP_016856971.1:p.Arg607Trp
XM_017001483.2:c.1732C>T XP_016856972.1:p.Arg578Trp
XM_024447661.1:c.1819C>T XP_024303429.1:p.Arg607Trp
XM_024447663.1:c.1639C>T XP_024303431.1:p.Arg547Trp
XM_024447664.1:c.1555C>T XP_024303432.1:p.Arg519Trp
XR_002956806.1:n.1851C>T
XR_946667.1:n.1851C>T