Canonical Allele Identifier: CA2342575810

Gene: PRKCG

Linked Data

• dbSNP Id: rs2068597405
• gnomAD v4: 19-53882276-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882278del , CM000681.2:g.53882278del	GRCh38
NC_000019.9:g.54385532del , CM000681.1:g.54385532del	GRCh37
NC_000019.8:g.59077344del	NCBI36
NG_009114.1:g.5066del , LRG_669:g.5066del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-217del	ENSP00000507230.1:n.-217del
ENST00000682268.1:n.82del
ENST00000682902.1:n.86del
ENST00000683513.1:c.-217del	ENSP00000506809.1:n.-217del
ENST00000263431.4:c.-217del MANE Select	ENSP00000263431.3:n.-217del
ENST00000263431.3:c.-217del	ENSP00000263431.3:n.-217del
ENST00000419486.1:c.-404del	ENSP00000387919.2:n.-404del
ENST00000474397.5:c.-322-279del	ENSP00000471271.1:n.-322-279del
ENST00000479081.5:c.-322-279del	ENSP00000471544.1:n.-322-279del
NM_001316329.1:c.-217del	NP_001303258.1:n.-217del
NM_002739.3:c.-217del , LRG_669t1:c.-217del	NP_002730.1:n.-217del
NM_002739.4:c.-217del	NP_002730.1:n.-217del
NM_002739.5:c.-217del MANE Select	NP_002730.1:n.-217del
NM_001316329.2:c.-217del	NP_001303258.1:n.-217del