Canonical Allele Identifier: CA285124246

Gene: PLCG2

Linked Data

• dbSNP Id: rs775682190
• gnomAD v2: 16-81923159-CACTT-C
• gnomAD v3: 16-81889554-CACTT-C
• gnomAD v4: 16-81889554-CACTT-C
• MyVariant Identifiers: chr16:g.81923160_81923163del (hg19) ; chr16:g.81889555_81889558del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.81889556_81889559del , CM000678.2:g.81889556_81889559del	GRCh38
NC_000016.9:g.81923161_81923164del , CM000678.1:g.81923161_81923164del	GRCh37
NC_000016.8:g.80480662_80480665del	NCBI36
NG_032019.2:g.155460_155463del , LRG_376:g.155460_155463del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563193.2:c.867+283_867+286del	ENSP00000455533.2:n.867+283_867+286del
ENST00000697561.1:c.*296+283_*296+286del	ENSP00000513337.1:n.*296+283_*296+286del
ENST00000697562.1:c.867+283_867+286del	ENSP00000513338.1:n.867+283_867+286del
ENST00000697563.1:c.*713+283_*713+286del	ENSP00000513339.1:n.*713+283_*713+286del
ENST00000697564.1:c.750+283_750+286del	ENSP00000513340.1:n.750+283_750+286del
ENST00000697565.1:n.807+283_807+286del
ENST00000697581.1:c.*861+283_*861+286del	ENSP00000513346.1:n.*861+283_*861+286del
ENST00000697582.1:c.867+283_867+286del	ENSP00000513347.1:n.867+283_867+286del
ENST00000697583.1:c.666+283_666+286del	ENSP00000513349.1:n.666+283_666+286del
ENST00000697584.1:c.666+283_666+286del	ENSP00000513350.1:n.666+283_666+286del
ENST00000697585.1:c.666+283_666+286del	ENSP00000513351.1:n.666+283_666+286del
ENST00000697586.1:c.666+283_666+286del	ENSP00000513352.1:n.666+283_666+286del
ENST00000697587.1:c.666+283_666+286del	ENSP00000513353.1:n.666+283_666+286del
ENST00000564138.6:c.867+283_867+286del MANE Select	ENSP00000482457.1:n.867+283_867+286del
ENST00000359376.7:c.867+283_867+286del	ENSP00000352336.4:n.867+283_867+286del
ENST00000562605.5:n.61+157_61+160del
ENST00000563193.1:c.175+283_175+286del
ENST00000564138.5:c.867+283_867+286del	ENSP00000482457.1:n.867+283_867+286del
ENST00000567980.5:n.1111+283_1111+286del
NM_002661.4:c.867+283_867+286del	NP_002652.2:n.867+283_867+286del
XM_011523108.1:c.981+283_981+286del	XP_011521410.1:n.981+283_981+286del
NM_002661.5:c.867+283_867+286del MANE Select	NP_002652.2:n.867+283_867+286del