Canonical Allele Identifier: CA14288057

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81854298A>G , CM000678.2:g.81854298A>G	GRCh38
NC_000016.9:g.81887903A>G , CM000678.1:g.81887903A>G	GRCh37
NC_000016.8:g.80445404A>G	NCBI36
NG_032019.2:g.120202A>G , LRG_376:g.120202A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.194-146A>G MANE Select	NP_002652.2:n.194-146A>G
ENST00000564138.6:c.194-146A>G MANE Select	ENSP00000482457.1:n.194-146A>G
NM_002661.4:c.194-146A>G	NP_002652.2:n.194-146A>G
ENST00000359376.7:c.194-146A>G	ENSP00000352336.4:n.194-146A>G
ENST00000563193.2:c.194-146A>G	ENSP00000455533.2:n.194-146A>G
ENST00000564138.5:c.194-146A>G	ENSP00000482457.1:n.194-146A>G
ENST00000565054.5:c.194-146A>G	ENSP00000455956.1:n.194-146A>G
ENST00000565400.5:n.518-146A>G
ENST00000567980.5:n.438-146A>G
ENST00000569523.1:n.226-146A>G
ENST00000569929.5:n.324-146A>G
ENST00000697561.1:c.194-146A>G	ENSP00000513337.1:n.194-146A>G
ENST00000697562.1:c.194-146A>G	ENSP00000513338.1:n.194-146A>G
ENST00000697563.1:c.194-146A>G	ENSP00000513339.1:n.194-146A>G
ENST00000697564.1:c.194-146A>G	ENSP00000513340.1:n.194-146A>G
ENST00000697565.1:n.134-146A>G
ENST00000697581.1:c.*188-146A>G	ENSP00000513346.1:n.*188-146A>G
ENST00000697582.1:c.194-146A>G	ENSP00000513347.1:n.194-146A>G
ENST00000697583.1:c.-8-146A>G	ENSP00000513349.1:n.-8-146A>G
ENST00000697584.1:c.-8-146A>G	ENSP00000513350.1:n.-8-146A>G
ENST00000697585.1:c.-8-146A>G	ENSP00000513351.1:n.-8-146A>G
ENST00000697586.1:c.-8-146A>G	ENSP00000513352.1:n.-8-146A>G
ENST00000697587.1:c.-8-146A>G	ENSP00000513353.1:n.-8-146A>G
XM_011523108.1:c.308-146A>G	XP_011521410.1:n.308-146A>G