Canonical Allele Identifier: CA2576074222

Gene: PLCG2

Linked Data

• gnomAD v4: 16-81889178-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889181del , CM000678.2:g.81889181del	GRCh38
NC_000016.9:g.81922786del , CM000678.1:g.81922786del	GRCh37
NC_000016.8:g.80480287del	NCBI36
NG_032019.2:g.155085del , LRG_376:g.155085del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.775del	ENSP00000455533.2:p.Ala259LeufsTer4
ENST00000697561.1:c.*204del	ENSP00000513337.1:n.*204del
ENST00000697562.1:c.775del	ENSP00000513338.1:p.Ala259LeufsTer4
ENST00000697563.1:c.*621del	ENSP00000513339.1:n.*621del
ENST00000697564.1:c.658del	ENSP00000513340.1:p.Ala220LeufsTer4
ENST00000697565.1:n.715del
ENST00000697581.1:c.*769del	ENSP00000513346.1:n.*769del
ENST00000697582.1:c.775del	ENSP00000513347.1:p.Ala259LeufsTer4
ENST00000697583.1:c.574del	ENSP00000513349.1:p.Ala192LeufsTer4
ENST00000697584.1:c.574del	ENSP00000513350.1:p.Ala192LeufsTer4
ENST00000697585.1:c.574del	ENSP00000513351.1:p.Ala192LeufsTer4
ENST00000697586.1:c.574del	ENSP00000513352.1:p.Ala192LeufsTer4
ENST00000697587.1:c.574del	ENSP00000513353.1:p.Ala192LeufsTer4
ENST00000564138.6:c.775del MANE Select	ENSP00000482457.1:p.Ala259LeufsTer4
ENST00000359376.7:c.775del	ENSP00000352336.4:p.Ala259LeufsTer4
ENST00000563193.1:c.83del
ENST00000564138.5:c.775del	ENSP00000482457.1:p.Ala259LeufsTer4
ENST00000567980.5:n.1019del
NM_002661.4:c.775del	NP_002652.2:p.Ala259LeufsTer4
XM_011523108.1:c.889del	XP_011521410.1:p.Ala297LeufsTer4
NM_002661.5:c.775del MANE Select	NP_002652.2:p.Ala259LeufsTer4