Canonical Allele Identifier: CA2237406840

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81928578A= , CM000678.2:g.81928578A=	GRCh38
NC_000016.9:g.81962183A= , CM000678.1:g.81962183A=	GRCh37
NC_000016.8:g.80519684A=	NCBI36
NG_032019.2:g.194482A= , LRG_376:g.194482A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.2535A= MANE Select	NP_002652.2:p.Leu845=
ENST00000564138.6:c.2535A= MANE Select	ENSP00000482457.1:p.Leu845=
NM_002661.4:c.2535A=	NP_002652.2:p.Leu845=
ENST00000359376.7:c.2535A=	ENSP00000352336.4:p.Leu845=
ENST00000564138.5:c.2535A=	ENSP00000482457.1:p.Leu845=
ENST00000570196.1:n.298A=
ENST00000570198.2:n.1653A=
ENST00000697562.1:c.*1395A=	ENSP00000513338.1:n.*1395A=
ENST00000697563.1:c.*2381A=	ENSP00000513339.1:n.*2381A=
ENST00000697564.1:c.2418A=	ENSP00000513340.1:p.Leu806=
ENST00000697581.1:c.*2529A=	ENSP00000513346.1:n.*2529A=
ENST00000697582.1:c.2535A=	ENSP00000513347.1:p.Leu845=
ENST00000697583.1:c.2334A=	ENSP00000513349.1:p.Leu778=
ENST00000697584.1:c.2334A=	ENSP00000513350.1:p.Leu778=
ENST00000697585.1:c.2334A=	ENSP00000513351.1:p.Leu778=
ENST00000697586.1:c.2334A=	ENSP00000513352.1:p.Leu778=
ENST00000697587.1:c.2334A=	ENSP00000513353.1:p.Leu778=
XM_011523108.1:c.2649A=	XP_011521410.1:p.Leu883=