Canonical Allele Identifier: CA8194411

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81931673G>A , CM000678.2:g.81931673G>A	GRCh38
NC_000016.9:g.81965278G>A , CM000678.1:g.81965278G>A	GRCh37
NC_000016.8:g.80522779G>A	NCBI36
NG_032019.2:g.197577G>A , LRG_376:g.197577G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.2739+19G>A MANE Select	NP_002652.2:n.2739+19G>A
ENST00000564138.6:c.2739+19G>A MANE Select	ENSP00000482457.1:n.2739+19G>A
NM_002661.4:c.2739+19G>A	NP_002652.2:n.2739+19G>A
ENST00000359376.7:c.2739+19G>A	ENSP00000352336.4:n.2739+19G>A
ENST00000563269.1:n.394+19G>A
ENST00000563269.2:n.914+19G>A
ENST00000564138.5:c.2739+19G>A	ENSP00000482457.1:n.2739+19G>A
ENST00000570198.2:n.1857+19G>A
ENST00000697562.1:c.*1599+19G>A	ENSP00000513338.1:n.*1599+19G>A
ENST00000697563.1:c.*2585+19G>A	ENSP00000513339.1:n.*2585+19G>A
ENST00000697564.1:c.2622+19G>A	ENSP00000513340.1:n.2622+19G>A
ENST00000697581.1:c.*2733+19G>A	ENSP00000513346.1:n.*2733+19G>A
ENST00000697582.1:c.2739+19G>A	ENSP00000513347.1:n.2739+19G>A
ENST00000697583.1:c.2538+19G>A	ENSP00000513349.1:n.2538+19G>A
ENST00000697584.1:c.2538+19G>A	ENSP00000513350.1:n.2538+19G>A
ENST00000697585.1:c.2538+19G>A	ENSP00000513351.1:n.2538+19G>A
ENST00000697586.1:c.2538+19G>A	ENSP00000513352.1:n.2538+19G>A
ENST00000697587.1:c.2538+19G>A	ENSP00000513353.1:n.2538+19G>A
XM_011523108.1:c.2853+19G>A	XP_011521410.1:n.2853+19G>A