Canonical Allele Identifier: CA8194708

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81939992A>G , CM000678.2:g.81939992A>G	GRCh38
NC_000016.9:g.81973597A>G , CM000678.1:g.81973597A>G	GRCh37
NC_000016.8:g.80531098A>G	NCBI36
NG_032019.2:g.205896A>G , LRG_376:g.205896A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563269.2:n.1589A>G
ENST00000570198.2:n.2532A>G
ENST00000697562.1:c.*2274A>G	ENSP00000513338.1:n.*2274A>G
ENST00000697563.1:c.*3260A>G	ENSP00000513339.1:n.*3260A>G
ENST00000697564.1:c.3297A>G	ENSP00000513340.1:p.Glu1099=
ENST00000697581.1:c.*3408A>G	ENSP00000513346.1:n.*3408A>G
ENST00000697582.1:c.*696A>G	ENSP00000513347.1:n.*696A>G
ENST00000697583.1:c.3213A>G	ENSP00000513349.1:p.Glu1071=
ENST00000697584.1:c.3213A>G	ENSP00000513350.1:p.Glu1071=
ENST00000697585.1:c.3213A>G	ENSP00000513351.1:p.Glu1071=
ENST00000697586.1:c.3213A>G	ENSP00000513352.1:p.Glu1071=
ENST00000697587.1:c.3213A>G	ENSP00000513353.1:p.Glu1071=
ENST00000564138.6:c.3414A>G MANE Select	ENSP00000482457.1:p.Glu1138=
ENST00000359376.7:c.3414A>G	ENSP00000352336.4:p.Glu1138=
ENST00000564138.5:c.3414A>G	ENSP00000482457.1:p.Glu1138=
ENST00000567356.1:n.389A>G
ENST00000567373.5:n.773A>G
NM_002661.4:c.3414A>G	NP_002652.2:p.Glu1138=
XM_011523108.1:c.3528A>G	XP_011521410.1:p.Glu1176=
NM_002661.5:c.3414A>G MANE Select	NP_002652.2:p.Glu1138=