Canonical Allele Identifier: CA8194159

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81921224C>T , CM000678.2:g.81921224C>T	GRCh38
NC_000016.9:g.81954829C>T , CM000678.1:g.81954829C>T	GRCh37
NC_000016.8:g.80512330C>T	NCBI36
NG_032019.2:g.187128C>T , LRG_376:g.187128C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570198.2:n.1380C>T
ENST00000697562.1:c.*1122C>T	ENSP00000513338.1:n.*1122C>T
ENST00000697563.1:c.*2108C>T	ENSP00000513339.1:n.*2108C>T
ENST00000697564.1:c.2145C>T	ENSP00000513340.1:p.Asp715=
ENST00000697581.1:c.*2256C>T	ENSP00000513346.1:n.*2256C>T
ENST00000697582.1:c.2262C>T	ENSP00000513347.1:p.Asp754=
ENST00000697583.1:c.2061C>T	ENSP00000513349.1:p.Asp687=
ENST00000697584.1:c.2061C>T	ENSP00000513350.1:p.Asp687=
ENST00000697585.1:c.2061C>T	ENSP00000513351.1:p.Asp687=
ENST00000697586.1:c.2061C>T	ENSP00000513352.1:p.Asp687=
ENST00000697587.1:c.2061C>T	ENSP00000513353.1:p.Asp687=
ENST00000564138.6:c.2262C>T MANE Select	ENSP00000482457.1:p.Asp754=
ENST00000359376.7:c.2262C>T	ENSP00000352336.4:p.Asp754=
ENST00000564138.5:c.2262C>T	ENSP00000482457.1:p.Asp754=
ENST00000567980.5:n.2506C>T
NM_002661.4:c.2262C>T	NP_002652.2:p.Asp754=
XM_011523108.1:c.2376C>T	XP_011521410.1:p.Asp792=
NM_002661.5:c.2262C>T MANE Select	NP_002652.2:p.Asp754=