Canonical Allele Identifier: CA16617216
Gene: PIK3CD HGNC NCBI

Linked Data

ClinVar Variation Id: 422410
dbSNP Id: rs1064795762

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9726985A>G , CM000663.2:g.9726985A>G GRCh38
NC_000001.10:g.9787043A>G , CM000663.1:g.9787043A>G GRCh37
NC_000001.9:g.9709630A>G NCBI36
NG_023434.1:g.80254A>G , LRG_191:g.80254A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000481137.2:c.*2328A>G ENSP00000513886.1:n.*2328A>G
ENST00000698709.1:c.2978A>G ENSP00000513887.1:p.Glu993Gly
ENST00000698710.1:c.3071A>G ENSP00000513888.1:p.Glu1024Gly
ENST00000698712.1:c.3074A>G ENSP00000513889.1:p.Glu1025Gly
ENST00000698713.1:c.3074A>G ENSP00000513890.1:p.Glu1025Gly
ENST00000698714.1:c.2930A>G ENSP00000513891.1:p.Glu977Gly
ENST00000698715.1:c.3071A>G ENSP00000513892.1:p.Glu1024Gly
ENST00000698716.1:c.3062A>G ENSP00000513893.1:p.Glu1021Gly
ENST00000698719.1:n.2235A>G
ENST00000377346.9:c.3074A>G MANE Select ENSP00000366563.4:p.Glu1025Gly
ENST00000361110.6:c.3146A>G ENSP00000354410.2:p.Glu1049Gly
ENST00000377346.8:c.3074A>G ENSP00000366563.4:p.Glu1025Gly
ENST00000536656.5:c.3146A>G ENSP00000446444.2:p.Glu1049Gly
ENST00000543390.2:c.3146A>G ENSP00000443811.2:p.Glu1049Gly
ENST00000628140.2:c.3146A>G ENSP00000486826.1:p.Glu1049Gly
NM_005026.3:c.3074A>G , LRG_191t1:c.3074A>G NP_005017.3:p.Glu1025Gly
XM_005263473.1:c.3071A>G XP_005263530.1:p.Glu1024Gly
XM_006710686.1:c.3074A>G XP_006710749.1:p.Glu1025Gly
XM_006710687.1:c.3074A>G XP_006710750.1:p.Glu1025Gly
XM_006710688.1:c.3074A>G XP_006710751.1:p.Glu1025Gly
XM_006710689.1:c.3074A>G XP_006710752.1:p.Glu1025Gly
XM_006710690.1:c.2987A>G XP_006710753.1:p.Glu996Gly
XM_011541581.1:c.3074A>G XP_011539883.1:p.Glu1025Gly
XM_011541582.1:c.2930A>G XP_011539884.1:p.Glu977Gly
XM_011541583.1:c.2426A>G XP_011539885.1:p.Glu809Gly
XR_946667.1:n.3159A>G
NM_001350234.1:c.3071A>G NP_001337163.1:p.Glu1024Gly
NM_001350235.1:c.2987A>G NP_001337164.1:p.Glu996Gly
NM_005026.4:c.3074A>G NP_005017.3:p.Glu1025Gly
XM_006710687.2:c.3074A>G XP_006710750.1:p.Glu1025Gly
XM_006710689.2:c.3074A>G XP_006710752.1:p.Glu1025Gly
XM_017001476.1:c.3251A>G XP_016856965.1:p.Glu1084Gly
XM_017001477.1:c.3251A>G XP_016856966.1:p.Glu1084Gly
XM_017001478.1:c.3251A>G XP_016856967.1:p.Glu1084Gly
XM_017001479.1:c.3251A>G XP_016856968.1:p.Glu1084Gly
XM_017001480.1:c.3251A>G XP_016856969.1:p.Glu1084Gly
XM_017001481.1:c.3251A>G XP_016856970.1:p.Glu1084Gly
XM_017001482.2:c.3251A>G XP_016856971.1:p.Glu1084Gly
XM_017001483.2:c.3164A>G XP_016856972.1:p.Glu1055Gly
XM_024447661.1:c.3251A>G XP_024303429.1:p.Glu1084Gly
XM_024447663.1:c.3071A>G XP_024303431.1:p.Glu1024Gly
XM_024447664.1:c.2987A>G XP_024303432.1:p.Glu996Gly
XR_002956806.1:n.3159A>G
NM_001350234.2:c.3071A>G NP_001337163.1:p.Glu1024Gly
NM_005026.5:c.3074A>G MANE Select NP_005017.3:p.Glu1025Gly