Canonical Allele Identifier: CA8194809

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81956850C>A , CM000678.2:g.81956850C>A	GRCh38
NC_000016.9:g.81990455C>A , CM000678.1:g.81990455C>A	GRCh37
NC_000016.8:g.80547956C>A	NCBI36
NG_032019.2:g.222754C>A , LRG_376:g.222754C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563269.2:n.1901C>A
ENST00000570198.2:n.2844C>A
ENST00000697562.1:c.*2586C>A	ENSP00000513338.1:n.*2586C>A
ENST00000697563.1:c.*3572C>A	ENSP00000513339.1:n.*3572C>A
ENST00000697564.1:c.3609C>A	ENSP00000513340.1:p.Leu1203=
ENST00000697581.1:c.*3720C>A	ENSP00000513346.1:n.*3720C>A
ENST00000697582.1:c.*1008C>A	ENSP00000513347.1:n.*1008C>A
ENST00000697583.1:c.3525C>A	ENSP00000513349.1:p.Leu1175=
ENST00000697584.1:c.3525C>A	ENSP00000513350.1:p.Leu1175=
ENST00000697585.1:c.3525C>A	ENSP00000513351.1:p.Leu1175=
ENST00000697586.1:c.3525C>A	ENSP00000513352.1:p.Leu1175=
ENST00000697587.1:c.3525C>A	ENSP00000513353.1:p.Leu1175=
ENST00000564138.6:c.3726C>A MANE Select	ENSP00000482457.1:p.Leu1242=
ENST00000359376.7:c.3725C>A	ENSP00000352336.4:p.Ser1242Tyr
ENST00000564138.5:c.3726C>A	ENSP00000482457.1:p.Leu1242=
NM_002661.4:c.3726C>A	NP_002652.2:p.Leu1242=
XM_011523108.1:c.3840C>A	XP_011521410.1:p.Leu1280=
NM_002661.5:c.3726C>A MANE Select	NP_002652.2:p.Leu1242=