Canonical Allele Identifier: CA2237371912

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889228T= , CM000678.2:g.81889228T=	GRCh38
NC_000016.9:g.81922833T= , CM000678.1:g.81922833T=	GRCh37
NC_000016.8:g.80480334T=	NCBI36
NG_032019.2:g.155132T= , LRG_376:g.155132T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.822T=	ENSP00000455533.2:p.Asp274=
ENST00000697561.1:c.*251T=	ENSP00000513337.1:n.*251T=
ENST00000697562.1:c.822T=	ENSP00000513338.1:p.Asp274=
ENST00000697563.1:c.*668T=	ENSP00000513339.1:n.*668T=
ENST00000697564.1:c.705T=	ENSP00000513340.1:p.Asp235=
ENST00000697565.1:n.762T=
ENST00000697581.1:c.*816T=	ENSP00000513346.1:n.*816T=
ENST00000697582.1:c.822T=	ENSP00000513347.1:p.Asp274=
ENST00000697583.1:c.621T=	ENSP00000513349.1:p.Asp207=
ENST00000697584.1:c.621T=	ENSP00000513350.1:p.Asp207=
ENST00000697585.1:c.621T=	ENSP00000513351.1:p.Asp207=
ENST00000697586.1:c.621T=	ENSP00000513352.1:p.Asp207=
ENST00000697587.1:c.621T=	ENSP00000513353.1:p.Asp207=
ENST00000564138.6:c.822T= MANE Select	ENSP00000482457.1:p.Asp274=
ENST00000359376.7:c.822T=	ENSP00000352336.4:p.Asp274=
ENST00000563193.1:c.130T=
ENST00000564138.5:c.822T=	ENSP00000482457.1:p.Asp274=
ENST00000567980.5:n.1066T=
NM_002661.4:c.822T=	NP_002652.2:p.Asp274=
XM_011523108.1:c.936T=	XP_011521410.1:p.Asp312=
NM_002661.5:c.822T= MANE Select	NP_002652.2:p.Asp274=