Canonical Allele Identifier: CA285173026
Gene: PLCG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81858090_81858096del , CM000678.2:g.81858090_81858096del GRCh38
NC_000016.9:g.81891695_81891701del , CM000678.1:g.81891695_81891701del GRCh37
NC_000016.8:g.80449196_80449202del NCBI36
NG_032019.2:g.123994_124000del , LRG_376:g.123994_124000del

Transcript Alleles

HGVS Amino-acid Change
ENST00000563193.2:c.338-173_338-167del ENSP00000455533.2:n.338-173_338-167del
ENST00000697561.1:c.338-173_338-167del ENSP00000513337.1:n.338-173_338-167del
ENST00000697562.1:c.338-173_338-167del ENSP00000513338.1:n.338-173_338-167del
ENST00000697563.1:c.338-1026_338-1020del ENSP00000513339.1:n.338-1026_338-1020del
ENST00000697564.1:c.338-173_338-167del ENSP00000513340.1:n.338-173_338-167del
ENST00000697565.1:n.278-173_278-167del
ENST00000697581.1:c.*332-173_*332-167del ENSP00000513346.1:n.*332-173_*332-167del
ENST00000697582.1:c.338-173_338-167del ENSP00000513347.1:n.338-173_338-167del
ENST00000697583.1:c.137-173_137-167del ENSP00000513349.1:n.137-173_137-167del
ENST00000697584.1:c.137-173_137-167del ENSP00000513350.1:n.137-173_137-167del
ENST00000697585.1:c.137-173_137-167del ENSP00000513351.1:n.137-173_137-167del
ENST00000697586.1:c.137-173_137-167del ENSP00000513352.1:n.137-173_137-167del
ENST00000697587.1:c.137-173_137-167del ENSP00000513353.1:n.137-173_137-167del
ENST00000564138.6:c.338-173_338-167del MANE Select ENSP00000482457.1:n.338-173_338-167del
ENST00000359376.7:c.338-173_338-167del ENSP00000352336.4:n.338-173_338-167del
ENST00000564138.5:c.338-173_338-167del ENSP00000482457.1:n.338-173_338-167del
ENST00000565020.1:n.146_152del
ENST00000565054.5:c.338-173_338-167del ENSP00000455956.1:n.338-173_338-167del
ENST00000565400.5:n.662-173_662-167del
ENST00000567980.5:n.582-173_582-167del
ENST00000569523.1:n.370-173_370-167del
ENST00000569929.5:n.468-1026_468-1020del
NM_002661.4:c.338-173_338-167del NP_002652.2:n.338-173_338-167del
XM_011523108.1:c.452-173_452-167del XP_011521410.1:n.452-173_452-167del
NM_002661.5:c.338-173_338-167del MANE Select NP_002652.2:n.338-173_338-167del