Canonical Allele Identifier: CA8194089

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81919524G>A , CM000678.2:g.81919524G>A	GRCh38
NC_000016.9:g.81953129G>A , CM000678.1:g.81953129G>A	GRCh37
NC_000016.8:g.80510630G>A	NCBI36
NG_032019.2:g.185428G>A , LRG_376:g.185428G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.2095G>A MANE Select	NP_002652.2:p.Gly699Ser
ENST00000564138.6:c.2095G>A MANE Select	ENSP00000482457.1:p.Gly699Ser
NM_002661.4:c.2095G>A	NP_002652.2:p.Gly699Ser
ENST00000359376.7:c.2095G>A	ENSP00000352336.4:p.Gly699Ser
ENST00000564138.5:c.2095G>A	ENSP00000482457.1:p.Gly699Ser
ENST00000567980.5:n.2339G>A
ENST00000570198.2:n.1213G>A
ENST00000697562.1:c.*955G>A	ENSP00000513338.1:n.*955G>A
ENST00000697563.1:c.*1941G>A	ENSP00000513339.1:n.*1941G>A
ENST00000697564.1:c.1978G>A	ENSP00000513340.1:p.Gly660Ser
ENST00000697581.1:c.*2089G>A	ENSP00000513346.1:n.*2089G>A
ENST00000697582.1:c.2095G>A	ENSP00000513347.1:p.Gly699Ser
ENST00000697583.1:c.1894G>A	ENSP00000513349.1:p.Gly632Ser
ENST00000697584.1:c.1894G>A	ENSP00000513350.1:p.Gly632Ser
ENST00000697585.1:c.1894G>A	ENSP00000513351.1:p.Gly632Ser
ENST00000697586.1:c.1894G>A	ENSP00000513352.1:p.Gly632Ser
ENST00000697587.1:c.1894G>A	ENSP00000513353.1:p.Gly632Ser
XM_011523108.1:c.2209G>A	XP_011521410.1:p.Gly737Ser