Canonical Allele Identifier: CA8193023

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81786086T>C , CM000678.2:g.81786086T>C	GRCh38
NC_000016.9:g.81819691T>C , CM000678.1:g.81819691T>C	GRCh37
NC_000016.8:g.80377192T>C	NCBI36
NG_032019.2:g.51990T>C , LRG_376:g.51990T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.97T>C MANE Select	NP_002652.2:p.Phe33Leu
ENST00000564138.6:c.97T>C MANE Select	ENSP00000482457.1:p.Phe33Leu
NM_002661.4:c.97T>C	NP_002652.2:p.Phe33Leu
ENST00000359376.7:c.97T>C	ENSP00000352336.4:p.Phe33Leu
ENST00000563193.2:c.97T>C	ENSP00000455533.2:p.Phe33Leu
ENST00000564138.5:c.97T>C	ENSP00000482457.1:p.Phe33Leu
ENST00000565054.5:c.97T>C	ENSP00000455956.1:p.Phe33Leu
ENST00000567980.5:n.341T>C
ENST00000569929.5:n.227T>C
ENST00000697561.1:c.97T>C	ENSP00000513337.1:p.Phe33Leu
ENST00000697562.1:c.97T>C	ENSP00000513338.1:p.Phe33Leu
ENST00000697563.1:c.97T>C	ENSP00000513339.1:p.Phe33Leu
ENST00000697564.1:c.97T>C	ENSP00000513340.1:p.Phe33Leu
ENST00000697565.1:n.37T>C
ENST00000697581.1:c.97T>C	ENSP00000513346.1:p.Phe33Leu
ENST00000697582.1:c.97T>C	ENSP00000513347.1:p.Phe33Leu