Canonical Allele Identifier: CA8194119

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81919640C>A , CM000678.2:g.81919640C>A	GRCh38
NC_000016.9:g.81953245C>A , CM000678.1:g.81953245C>A	GRCh37
NC_000016.8:g.80510746C>A	NCBI36
NG_032019.2:g.185544C>A , LRG_376:g.185544C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.2211C>A MANE Select	NP_002652.2:p.Pro737=
ENST00000564138.6:c.2211C>A MANE Select	ENSP00000482457.1:p.Pro737=
NM_002661.4:c.2211C>A	NP_002652.2:p.Pro737=
ENST00000359376.7:c.2211C>A	ENSP00000352336.4:p.Pro737=
ENST00000564138.5:c.2211C>A	ENSP00000482457.1:p.Pro737=
ENST00000567980.5:n.2455C>A
ENST00000570198.2:n.1329C>A
ENST00000697562.1:c.*1071C>A	ENSP00000513338.1:n.*1071C>A
ENST00000697563.1:c.*2057C>A	ENSP00000513339.1:n.*2057C>A
ENST00000697564.1:c.2094C>A	ENSP00000513340.1:p.Pro698=
ENST00000697581.1:c.*2205C>A	ENSP00000513346.1:n.*2205C>A
ENST00000697582.1:c.2211C>A	ENSP00000513347.1:p.Pro737=
ENST00000697583.1:c.2010C>A	ENSP00000513349.1:p.Pro670=
ENST00000697584.1:c.2010C>A	ENSP00000513350.1:p.Pro670=
ENST00000697585.1:c.2010C>A	ENSP00000513351.1:p.Pro670=
ENST00000697586.1:c.2010C>A	ENSP00000513352.1:p.Pro670=
ENST00000697587.1:c.2010C>A	ENSP00000513353.1:p.Pro670=
XM_011523108.1:c.2325C>A	XP_011521410.1:p.Pro775=