Canonical Allele Identifier: CA8194751

Gene: PLCG2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81946186G>A , CM000678.2:g.81946186G>A	GRCh38
NC_000016.9:g.81979791G>A , CM000678.1:g.81979791G>A	GRCh37
NC_000016.8:g.80537292G>A	NCBI36
NG_032019.2:g.212090G>A , LRG_376:g.212090G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002661.5:c.3493G>A MANE Select	NP_002652.2:p.Val1165Ile
ENST00000564138.6:c.3493G>A MANE Select	ENSP00000482457.1:p.Val1165Ile
NM_002661.4:c.3493G>A	NP_002652.2:p.Val1165Ile
ENST00000359376.7:c.3493G>A	ENSP00000352336.4:p.Val1165Ile
ENST00000563269.2:n.1668G>A
ENST00000564138.5:c.3493G>A	ENSP00000482457.1:p.Val1165Ile
ENST00000567356.1:n.468G>A
ENST00000570198.2:n.2611G>A
ENST00000697562.1:c.*2353G>A	ENSP00000513338.1:n.*2353G>A
ENST00000697563.1:c.*3339G>A	ENSP00000513339.1:n.*3339G>A
ENST00000697564.1:c.3376G>A	ENSP00000513340.1:p.Val1126Ile
ENST00000697581.1:c.*3487G>A	ENSP00000513346.1:n.*3487G>A
ENST00000697582.1:c.*775G>A	ENSP00000513347.1:n.*775G>A
ENST00000697583.1:c.3292G>A	ENSP00000513349.1:p.Val1098Ile
ENST00000697584.1:c.3292G>A	ENSP00000513350.1:p.Val1098Ile
ENST00000697585.1:c.3292G>A	ENSP00000513351.1:p.Val1098Ile
ENST00000697586.1:c.3292G>A	ENSP00000513352.1:p.Val1098Ile
ENST00000697587.1:c.3292G>A	ENSP00000513353.1:p.Val1098Ile
XM_011523108.1:c.3607G>A	XP_011521410.1:p.Val1203Ile