Canonical Allele Identifier: CA2237372074
Gene: PLCG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81889336_81889337delinsAG , CM000678.2:g.81889336_81889337delinsAG GRCh38
NC_000016.9:g.81922941_81922942delinsAG , CM000678.1:g.81922941_81922942delinsAG GRCh37
NC_000016.8:g.80480442_80480443delinsAG NCBI36
NG_032019.2:g.155240_155241delinsAG , LRG_376:g.155240_155241delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000563193.2:c.867+63_867+64delinsAG ENSP00000455533.2:n.867+63_867+64delinsAG
ENST00000697561.1:c.*296+63_*296+64delinsAG ENSP00000513337.1:n.*296+63_*296+64delinsAG
ENST00000697562.1:c.867+63_867+64delinsAG ENSP00000513338.1:n.867+63_867+64delinsAG
ENST00000697563.1:c.*713+63_*713+64delinsAG ENSP00000513339.1:n.*713+63_*713+64delinsAG
ENST00000697564.1:c.750+63_750+64delinsAG ENSP00000513340.1:n.750+63_750+64delinsAG
ENST00000697565.1:n.807+63_807+64delinsAG
ENST00000697581.1:c.*861+63_*861+64delinsAG ENSP00000513346.1:n.*861+63_*861+64delinsAG
ENST00000697582.1:c.867+63_867+64delinsAG ENSP00000513347.1:n.867+63_867+64delinsAG
ENST00000697583.1:c.666+63_666+64delinsAG ENSP00000513349.1:n.666+63_666+64delinsAG
ENST00000697584.1:c.666+63_666+64delinsAG ENSP00000513350.1:n.666+63_666+64delinsAG
ENST00000697585.1:c.666+63_666+64delinsAG ENSP00000513351.1:n.666+63_666+64delinsAG
ENST00000697586.1:c.666+63_666+64delinsAG ENSP00000513352.1:n.666+63_666+64delinsAG
ENST00000697587.1:c.666+63_666+64delinsAG ENSP00000513353.1:n.666+63_666+64delinsAG
ENST00000564138.6:c.867+63_867+64delinsAG MANE Select ENSP00000482457.1:n.867+63_867+64delinsAG
ENST00000359376.7:c.867+63_867+64delinsAG ENSP00000352336.4:n.867+63_867+64delinsAG
ENST00000563193.1:c.175+63_175+64delinsAG
ENST00000564138.5:c.867+63_867+64delinsAG ENSP00000482457.1:n.867+63_867+64delinsAG
ENST00000567980.5:n.1111+63_1111+64delinsAG
NM_002661.4:c.867+63_867+64delinsAG NP_002652.2:n.867+63_867+64delinsAG
XM_011523108.1:c.981+63_981+64delinsAG XP_011521410.1:n.981+63_981+64delinsAG
NM_002661.5:c.867+63_867+64delinsAG MANE Select NP_002652.2:n.867+63_867+64delinsAG