Canonical Allele Identifier: CA2237378279

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81912655C= , CM000678.2:g.81912655C=	GRCh38
NC_000016.9:g.81946260C= , CM000678.1:g.81946260C=	GRCh37
NC_000016.8:g.80503761C=	NCBI36
NG_032019.2:g.178559C= , LRG_376:g.178559C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.1993C= MANE Select	NP_002652.2:p.Arg665=
ENST00000564138.6:c.1993C= MANE Select	ENSP00000482457.1:p.Arg665=
NM_002661.4:c.1993C=	NP_002652.2:p.Arg665=
ENST00000359376.7:c.1993C=	ENSP00000352336.4:p.Arg665=
ENST00000564138.5:c.1993C=	ENSP00000482457.1:p.Arg665=
ENST00000567980.5:n.2237C=
ENST00000570198.2:n.1111C=
ENST00000697562.1:c.*853C=	ENSP00000513338.1:n.*853C=
ENST00000697563.1:c.*1839C=	ENSP00000513339.1:n.*1839C=
ENST00000697564.1:c.1876C=	ENSP00000513340.1:p.Arg626=
ENST00000697581.1:c.*1987C=	ENSP00000513346.1:n.*1987C=
ENST00000697582.1:c.1993C=	ENSP00000513347.1:p.Arg665=
ENST00000697583.1:c.1792C=	ENSP00000513349.1:p.Arg598=
ENST00000697584.1:c.1792C=	ENSP00000513350.1:p.Arg598=
ENST00000697585.1:c.1792C=	ENSP00000513351.1:p.Arg598=
ENST00000697586.1:c.1792C=	ENSP00000513352.1:p.Arg598=
ENST00000697587.1:c.1792C=	ENSP00000513353.1:p.Arg598=
XM_011523108.1:c.2107C=	XP_011521410.1:p.Arg703=