Canonical Allele Identifier: CA2586962487

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53882355-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882357del , CM000681.2:g.53882357del	GRCh38
NC_000019.9:g.54385611del , CM000681.1:g.54385611del	GRCh37
NC_000019.8:g.59077423del	NCBI36
NG_009114.1:g.5145del , LRG_669:g.5145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-138del	ENSP00000507230.1:n.-138del
ENST00000682268.1:n.161del
ENST00000682902.1:n.165del
ENST00000683513.1:c.-138del	ENSP00000506809.1:n.-138del
ENST00000263431.4:c.-138del MANE Select	ENSP00000263431.3:n.-138del
ENST00000263431.3:c.-138del	ENSP00000263431.3:n.-138del
ENST00000419486.1:c.-325del	ENSP00000387919.2:n.-325del
ENST00000474397.5:c.-322-200del	ENSP00000471271.1:n.-322-200del
ENST00000479081.5:c.-322-200del	ENSP00000471544.1:n.-322-200del
NM_001316329.1:c.-138del	NP_001303258.1:n.-138del
NM_002739.3:c.-138del , LRG_669t1:c.-138del	NP_002730.1:n.-138del
NM_002739.4:c.-138del	NP_002730.1:n.-138del
NM_002739.5:c.-138del MANE Select	NP_002730.1:n.-138del
NM_001316329.2:c.-138del	NP_001303258.1:n.-138del