Canonical Allele Identifier: CA2237371991

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889264T= , CM000678.2:g.81889264T=	GRCh38
NC_000016.9:g.81922869T= , CM000678.1:g.81922869T=	GRCh37
NC_000016.8:g.80480370T=	NCBI36
NG_032019.2:g.155168T= , LRG_376:g.155168T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.858T=	ENSP00000455533.2:p.Phe286=
ENST00000697561.1:c.*287T=	ENSP00000513337.1:n.*287T=
ENST00000697562.1:c.858T=	ENSP00000513338.1:p.Phe286=
ENST00000697563.1:c.*704T=	ENSP00000513339.1:n.*704T=
ENST00000697564.1:c.741T=	ENSP00000513340.1:p.Phe247=
ENST00000697565.1:n.798T=
ENST00000697581.1:c.*852T=	ENSP00000513346.1:n.*852T=
ENST00000697582.1:c.858T=	ENSP00000513347.1:p.Phe286=
ENST00000697583.1:c.657T=	ENSP00000513349.1:p.Phe219=
ENST00000697584.1:c.657T=	ENSP00000513350.1:p.Phe219=
ENST00000697585.1:c.657T=	ENSP00000513351.1:p.Phe219=
ENST00000697586.1:c.657T=	ENSP00000513352.1:p.Phe219=
ENST00000697587.1:c.657T=	ENSP00000513353.1:p.Phe219=
ENST00000564138.6:c.858T= MANE Select	ENSP00000482457.1:p.Phe286=
ENST00000359376.7:c.858T=	ENSP00000352336.4:p.Phe286=
ENST00000563193.1:c.166T=
ENST00000564138.5:c.858T=	ENSP00000482457.1:p.Phe286=
ENST00000567980.5:n.1102T=
NM_002661.4:c.858T=	NP_002652.2:p.Phe286=
XM_011523108.1:c.972T=	XP_011521410.1:p.Phe324=
NM_002661.5:c.858T= MANE Select	NP_002652.2:p.Phe286=