Canonical Allele Identifier: CA2586962347

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53882260-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882264del , CM000681.2:g.53882264del	GRCh38
NC_000019.9:g.54385518del , CM000681.1:g.54385518del	GRCh37
NC_000019.8:g.59077330del	NCBI36
NG_009114.1:g.5052del , LRG_669:g.5052del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-231del	ENSP00000507230.1:n.-231del
ENST00000682268.1:n.68del
ENST00000682902.1:n.72del
ENST00000683513.1:c.-231del	ENSP00000506809.1:n.-231del
ENST00000263431.4:c.-231del MANE Select	ENSP00000263431.3:n.-231del
ENST00000263431.3:c.-231del	ENSP00000263431.3:n.-231del
ENST00000419486.1:c.-418del	ENSP00000387919.2:n.-418del
ENST00000474397.5:c.-322-293del	ENSP00000471271.1:n.-322-293del
ENST00000479081.5:c.-322-293del	ENSP00000471544.1:n.-322-293del
NM_001316329.1:c.-231del	NP_001303258.1:n.-231del
NM_002739.3:c.-231del , LRG_669t1:c.-231del	NP_002730.1:n.-231del
NM_002739.4:c.-231del	NP_002730.1:n.-231del
NM_002739.5:c.-231del MANE Select	NP_002730.1:n.-231del
NM_001316329.2:c.-231del	NP_001303258.1:n.-231del