Canonical Allele Identifier: CA2237371904

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889224T= , CM000678.2:g.81889224T=	GRCh38
NC_000016.9:g.81922829T= , CM000678.1:g.81922829T=	GRCh37
NC_000016.8:g.80480330T=	NCBI36
NG_032019.2:g.155128T= , LRG_376:g.155128T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.818T=	ENSP00000455533.2:p.Ile273=
ENST00000697561.1:c.*247T=	ENSP00000513337.1:n.*247T=
ENST00000697562.1:c.818T=	ENSP00000513338.1:p.Ile273=
ENST00000697563.1:c.*664T=	ENSP00000513339.1:n.*664T=
ENST00000697564.1:c.701T=	ENSP00000513340.1:p.Ile234=
ENST00000697565.1:n.758T=
ENST00000697581.1:c.*812T=	ENSP00000513346.1:n.*812T=
ENST00000697582.1:c.818T=	ENSP00000513347.1:p.Ile273=
ENST00000697583.1:c.617T=	ENSP00000513349.1:p.Ile206=
ENST00000697584.1:c.617T=	ENSP00000513350.1:p.Ile206=
ENST00000697585.1:c.617T=	ENSP00000513351.1:p.Ile206=
ENST00000697586.1:c.617T=	ENSP00000513352.1:p.Ile206=
ENST00000697587.1:c.617T=	ENSP00000513353.1:p.Ile206=
ENST00000564138.6:c.818T= MANE Select	ENSP00000482457.1:p.Ile273=
ENST00000359376.7:c.818T=	ENSP00000352336.4:p.Ile273=
ENST00000563193.1:c.126T=
ENST00000564138.5:c.818T=	ENSP00000482457.1:p.Ile273=
ENST00000567980.5:n.1062T=
NM_002661.4:c.818T=	NP_002652.2:p.Ile273=
XM_011523108.1:c.932T=	XP_011521410.1:p.Ile311=
NM_002661.5:c.818T= MANE Select	NP_002652.2:p.Ile273=