Canonical Allele Identifier: CA415876078

Gene: PIK3CD

Linked Data

• MyVariant Identifiers: chr1:g.9787044G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.9726986G>A , CM000663.2:g.9726986G>A	GRCh38
NC_000001.10:g.9787044G>A , CM000663.1:g.9787044G>A	GRCh37
NC_000001.9:g.9709631G>A	NCBI36
NG_023434.1:g.80255G>A , LRG_191:g.80255G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000481137.2:c.*2329G>A	ENSP00000513886.1:n.*2329G>A
ENST00000698709.1:c.2979G>A	ENSP00000513887.1:p.Glu993=
ENST00000698710.1:c.3072G>A	ENSP00000513888.1:p.Glu1024=
ENST00000698712.1:c.3075G>A	ENSP00000513889.1:p.Glu1025=
ENST00000698713.1:c.3075G>A	ENSP00000513890.1:p.Glu1025=
ENST00000698714.1:c.2931G>A	ENSP00000513891.1:p.Glu977=
ENST00000698715.1:c.3072G>A	ENSP00000513892.1:p.Glu1024=
ENST00000698716.1:c.3063G>A	ENSP00000513893.1:p.Glu1021=
ENST00000698719.1:n.2236G>A
ENST00000377346.9:c.3075G>A MANE Select	ENSP00000366563.4:p.Glu1025=
ENST00000361110.6:c.3147G>A	ENSP00000354410.2:p.Glu1049=
ENST00000377346.8:c.3075G>A	ENSP00000366563.4:p.Glu1025=
ENST00000536656.5:c.3147G>A	ENSP00000446444.2:p.Glu1049=
ENST00000543390.2:c.3147G>A	ENSP00000443811.2:p.Glu1049=
ENST00000628140.2:c.3147G>A	ENSP00000486826.1:p.Glu1049=
NM_005026.3:c.3075G>A , LRG_191t1:c.3075G>A	NP_005017.3:p.Glu1025=
XM_005263473.1:c.3072G>A	XP_005263530.1:p.Glu1024=
XM_006710686.1:c.3075G>A	XP_006710749.1:p.Glu1025=
XM_006710687.1:c.3075G>A	XP_006710750.1:p.Glu1025=
XM_006710688.1:c.3075G>A	XP_006710751.1:p.Glu1025=
XM_006710689.1:c.3075G>A	XP_006710752.1:p.Glu1025=
XM_006710690.1:c.2988G>A	XP_006710753.1:p.Glu996=
XM_011541581.1:c.3075G>A	XP_011539883.1:p.Glu1025=
XM_011541582.1:c.2931G>A	XP_011539884.1:p.Glu977=
XM_011541583.1:c.2427G>A	XP_011539885.1:p.Glu809=
XR_946667.1:n.3160G>A
NM_001350234.1:c.3072G>A	NP_001337163.1:p.Glu1024=
NM_001350235.1:c.2988G>A	NP_001337164.1:p.Glu996=
NM_005026.4:c.3075G>A	NP_005017.3:p.Glu1025=
XM_006710687.2:c.3075G>A	XP_006710750.1:p.Glu1025=
XM_006710689.2:c.3075G>A	XP_006710752.1:p.Glu1025=
XM_017001476.1:c.3252G>A	XP_016856965.1:p.Glu1084=
XM_017001477.1:c.3252G>A	XP_016856966.1:p.Glu1084=
XM_017001478.1:c.3252G>A	XP_016856967.1:p.Glu1084=
XM_017001479.1:c.3252G>A	XP_016856968.1:p.Glu1084=
XM_017001480.1:c.3252G>A	XP_016856969.1:p.Glu1084=
XM_017001481.1:c.3252G>A	XP_016856970.1:p.Glu1084=
XM_017001482.2:c.3252G>A	XP_016856971.1:p.Glu1084=
XM_017001483.2:c.3165G>A	XP_016856972.1:p.Glu1055=
XM_024447661.1:c.3252G>A	XP_024303429.1:p.Glu1084=
XM_024447663.1:c.3072G>A	XP_024303431.1:p.Glu1024=
XM_024447664.1:c.2988G>A	XP_024303432.1:p.Glu996=
XR_002956806.1:n.3160G>A
NM_001350234.2:c.3072G>A	NP_001337163.1:p.Glu1024=
NM_005026.5:c.3075G>A MANE Select	NP_005017.3:p.Glu1025=