Canonical Allele Identifier: CA577633

Gene: PIK3CD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.9724377T>C , CM000663.2:g.9724377T>C	GRCh38
NC_000001.10:g.9784435T>C , CM000663.1:g.9784435T>C	GRCh37
NC_000001.9:g.9707022T>C	NCBI36
NG_023434.1:g.77646T>C , LRG_191:g.77646T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481137.2:c.*2074T>C	ENSP00000513886.1:n.*2074T>C
ENST00000698709.1:c.2724T>C	ENSP00000513887.1:p.His908=
ENST00000698710.1:c.2817T>C	ENSP00000513888.1:p.His939=
ENST00000698712.1:c.2820T>C	ENSP00000513889.1:p.His940=
ENST00000698713.1:c.2820T>C	ENSP00000513890.1:p.His940=
ENST00000698714.1:c.2676T>C	ENSP00000513891.1:p.His892=
ENST00000698715.1:c.2817T>C	ENSP00000513892.1:p.His939=
ENST00000698716.1:c.2808T>C	ENSP00000513893.1:p.His936=
ENST00000698719.1:n.1981T>C
ENST00000377346.9:c.2820T>C MANE Select	ENSP00000366563.4:p.His940=
ENST00000361110.6:c.2892T>C	ENSP00000354410.2:p.His964=
ENST00000377346.8:c.2820T>C	ENSP00000366563.4:p.His940=
ENST00000536656.5:c.2892T>C	ENSP00000446444.2:p.His964=
ENST00000543390.2:c.2892T>C	ENSP00000443811.2:p.His964=
ENST00000628140.2:c.2892T>C	ENSP00000486826.1:p.His964=
NM_005026.3:c.2820T>C , LRG_191t1:c.2820T>C	NP_005017.3:p.His940=
XM_005263473.1:c.2817T>C	XP_005263530.1:p.His939=
XM_006710686.1:c.2820T>C	XP_006710749.1:p.His940=
XM_006710687.1:c.2820T>C	XP_006710750.1:p.His940=
XM_006710688.1:c.2820T>C	XP_006710751.1:p.His940=
XM_006710689.1:c.2820T>C	XP_006710752.1:p.His940=
XM_006710690.1:c.2733T>C	XP_006710753.1:p.His911=
XM_011541581.1:c.2820T>C	XP_011539883.1:p.His940=
XM_011541582.1:c.2676T>C	XP_011539884.1:p.His892=
XM_011541583.1:c.2172T>C	XP_011539885.1:p.His724=
XR_946667.1:n.2905T>C
NM_001350234.1:c.2817T>C	NP_001337163.1:p.His939=
NM_001350235.1:c.2733T>C	NP_001337164.1:p.His911=
NM_005026.4:c.2820T>C	NP_005017.3:p.His940=
XM_006710687.2:c.2820T>C	XP_006710750.1:p.His940=
XM_006710689.2:c.2820T>C	XP_006710752.1:p.His940=
XM_017001476.1:c.2997T>C	XP_016856965.1:p.His999=
XM_017001477.1:c.2997T>C	XP_016856966.1:p.His999=
XM_017001478.1:c.2997T>C	XP_016856967.1:p.His999=
XM_017001479.1:c.2997T>C	XP_016856968.1:p.His999=
XM_017001480.1:c.2997T>C	XP_016856969.1:p.His999=
XM_017001481.1:c.2997T>C	XP_016856970.1:p.His999=
XM_017001482.2:c.2997T>C	XP_016856971.1:p.His999=
XM_017001483.2:c.2910T>C	XP_016856972.1:p.His970=
XM_024447661.1:c.2997T>C	XP_024303429.1:p.His999=
XM_024447663.1:c.2817T>C	XP_024303431.1:p.His939=
XM_024447664.1:c.2733T>C	XP_024303432.1:p.His911=
XR_002956806.1:n.2905T>C
NM_001350234.2:c.2817T>C	NP_001337163.1:p.His939=
NM_005026.5:c.2820T>C MANE Select	NP_005017.3:p.His940=