Canonical Allele Identifier: CA8193807

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81907718G>T , CM000678.2:g.81907718G>T	GRCh38
NC_000016.9:g.81941323G>T , CM000678.1:g.81941323G>T	GRCh37
NC_000016.8:g.80498824G>T	NCBI36
NG_032019.2:g.173622G>T , LRG_376:g.173622G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570198.2:n.619G>T
ENST00000697562.1:c.*361G>T	ENSP00000513338.1:n.*361G>T
ENST00000697563.1:c.*1347G>T	ENSP00000513339.1:n.*1347G>T
ENST00000697564.1:c.1384G>T	ENSP00000513340.1:p.Ala462Ser
ENST00000697581.1:c.*1495G>T	ENSP00000513346.1:n.*1495G>T
ENST00000697582.1:c.1501G>T	ENSP00000513347.1:p.Ala501Ser
ENST00000697583.1:c.1300G>T	ENSP00000513349.1:p.Ala434Ser
ENST00000697584.1:c.1300G>T	ENSP00000513350.1:p.Ala434Ser
ENST00000697585.1:c.1300G>T	ENSP00000513351.1:p.Ala434Ser
ENST00000697586.1:c.1300G>T	ENSP00000513352.1:p.Ala434Ser
ENST00000697587.1:c.1300G>T	ENSP00000513353.1:p.Ala434Ser
ENST00000564138.6:c.1501G>T MANE Select	ENSP00000482457.1:p.Ala501Ser
ENST00000359376.7:c.1501G>T	ENSP00000352336.4:p.Ala501Ser
ENST00000564138.5:c.1501G>T	ENSP00000482457.1:p.Ala501Ser
ENST00000567980.5:n.1745G>T
NM_002661.4:c.1501G>T	NP_002652.2:p.Ala501Ser
XM_011523108.1:c.1615G>T	XP_011521410.1:p.Ala539Ser
NM_002661.5:c.1501G>T MANE Select	NP_002652.2:p.Ala501Ser