Canonical Allele Identifier: CA8193891

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81908570A>G , CM000678.2:g.81908570A>G	GRCh38
NC_000016.9:g.81942175A>G , CM000678.1:g.81942175A>G	GRCh37
NC_000016.8:g.80499676A>G	NCBI36
NG_032019.2:g.174474A>G , LRG_376:g.174474A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570198.2:n.830A>G
ENST00000697562.1:c.*572A>G	ENSP00000513338.1:n.*572A>G
ENST00000697563.1:c.*1558A>G	ENSP00000513339.1:n.*1558A>G
ENST00000697564.1:c.1595A>G	ENSP00000513340.1:p.Asn532Ser
ENST00000697581.1:c.*1706A>G	ENSP00000513346.1:n.*1706A>G
ENST00000697582.1:c.1712A>G	ENSP00000513347.1:p.Asn571Ser
ENST00000697583.1:c.1511A>G	ENSP00000513349.1:p.Asn504Ser
ENST00000697584.1:c.1511A>G	ENSP00000513350.1:p.Asn504Ser
ENST00000697585.1:c.1511A>G	ENSP00000513351.1:p.Asn504Ser
ENST00000697586.1:c.1511A>G	ENSP00000513352.1:p.Asn504Ser
ENST00000697587.1:c.1511A>G	ENSP00000513353.1:p.Asn504Ser
ENST00000564138.6:c.1712A>G MANE Select	ENSP00000482457.1:p.Asn571Ser
ENST00000359376.7:c.1712A>G	ENSP00000352336.4:p.Asn571Ser
ENST00000564138.5:c.1712A>G	ENSP00000482457.1:p.Asn571Ser
ENST00000567980.5:n.1956A>G
NM_002661.4:c.1712A>G	NP_002652.2:p.Asn571Ser
XM_011523108.1:c.1826A>G	XP_011521410.1:p.Asn609Ser
NM_002661.5:c.1712A>G MANE Select	NP_002652.2:p.Asn571Ser