Canonical Allele Identifier: CA396897779

Gene: PLCG2

Linked Data

• COSMIC: COSM4918876 ; COSM4918877
• MyVariant Identifiers: chr16:g.81922840A>T (hg19) ; chr16:g.81889235A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889235A>T , CM000678.2:g.81889235A>T	GRCh38
NC_000016.9:g.81922840A>T , CM000678.1:g.81922840A>T	GRCh37
NC_000016.8:g.80480341A>T	NCBI36
NG_032019.2:g.155139A>T , LRG_376:g.155139A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.829A>T	ENSP00000455533.2:p.Met277Leu
ENST00000697561.1:c.*258A>T	ENSP00000513337.1:n.*258A>T
ENST00000697562.1:c.829A>T	ENSP00000513338.1:p.Met277Leu
ENST00000697563.1:c.*675A>T	ENSP00000513339.1:n.*675A>T
ENST00000697564.1:c.712A>T	ENSP00000513340.1:p.Met238Leu
ENST00000697565.1:n.769A>T
ENST00000697581.1:c.*823A>T	ENSP00000513346.1:n.*823A>T
ENST00000697582.1:c.829A>T	ENSP00000513347.1:p.Met277Leu
ENST00000697583.1:c.628A>T	ENSP00000513349.1:p.Met210Leu
ENST00000697584.1:c.628A>T	ENSP00000513350.1:p.Met210Leu
ENST00000697585.1:c.628A>T	ENSP00000513351.1:p.Met210Leu
ENST00000697586.1:c.628A>T	ENSP00000513352.1:p.Met210Leu
ENST00000697587.1:c.628A>T	ENSP00000513353.1:p.Met210Leu
ENST00000564138.6:c.829A>T MANE Select	ENSP00000482457.1:p.Met277Leu
ENST00000359376.7:c.829A>T	ENSP00000352336.4:p.Met277Leu
ENST00000563193.1:c.137A>T
ENST00000564138.5:c.829A>T	ENSP00000482457.1:p.Met277Leu
ENST00000567980.5:n.1073A>T
NM_002661.4:c.829A>T	NP_002652.2:p.Met277Leu
XM_011523108.1:c.943A>T	XP_011521410.1:p.Met315Leu
NM_002661.5:c.829A>T MANE Select	NP_002652.2:p.Met277Leu