Canonical Allele Identifier: CA2634519862

Gene: PLCG2

Linked Data

• gnomAD v4: 16-81889432-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889438dup , CM000678.2:g.81889438dup	GRCh38
NC_000016.9:g.81923043dup , CM000678.1:g.81923043dup	GRCh37
NC_000016.8:g.80480544dup	NCBI36
NG_032019.2:g.155342dup , LRG_376:g.155342dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.867+165dup	ENSP00000455533.2:n.867+165dup
ENST00000697561.1:c.*296+165dup	ENSP00000513337.1:n.*296+165dup
ENST00000697562.1:c.867+165dup	ENSP00000513338.1:n.867+165dup
ENST00000697563.1:c.*713+165dup	ENSP00000513339.1:n.*713+165dup
ENST00000697564.1:c.750+165dup	ENSP00000513340.1:n.750+165dup
ENST00000697565.1:n.807+165dup
ENST00000697581.1:c.*861+165dup	ENSP00000513346.1:n.*861+165dup
ENST00000697582.1:c.867+165dup	ENSP00000513347.1:n.867+165dup
ENST00000697583.1:c.666+165dup	ENSP00000513349.1:n.666+165dup
ENST00000697584.1:c.666+165dup	ENSP00000513350.1:n.666+165dup
ENST00000697585.1:c.666+165dup	ENSP00000513351.1:n.666+165dup
ENST00000697586.1:c.666+165dup	ENSP00000513352.1:n.666+165dup
ENST00000697587.1:c.666+165dup	ENSP00000513353.1:n.666+165dup
ENST00000564138.6:c.867+165dup MANE Select	ENSP00000482457.1:n.867+165dup
ENST00000359376.7:c.867+165dup	ENSP00000352336.4:n.867+165dup
ENST00000562605.5:n.61+39dup
ENST00000563193.1:c.175+165dup
ENST00000564138.5:c.867+165dup	ENSP00000482457.1:n.867+165dup
ENST00000567980.5:n.1111+165dup
NM_002661.4:c.867+165dup	NP_002652.2:n.867+165dup
XM_011523108.1:c.981+165dup	XP_011521410.1:n.981+165dup
NM_002661.5:c.867+165dup MANE Select	NP_002652.2:n.867+165dup