Canonical Allele Identifier: CA2342575774

Gene: PRKCG

Linked Data

• dbSNP Id: rs2068596786

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882241del , CM000681.2:g.53882241del	GRCh38
NC_000019.9:g.54385495del , CM000681.1:g.54385495del	GRCh37
NC_000019.8:g.59077307del	NCBI36
NG_009114.1:g.5029del , LRG_669:g.5029del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-254del	ENSP00000507230.1:n.-254del
ENST00000682268.1:n.45del
ENST00000682902.1:n.49del
ENST00000683513.1:c.-254del	ENSP00000506809.1:n.-254del
ENST00000263431.4:c.-254del MANE Select	ENSP00000263431.3:n.-254del
ENST00000263431.3:c.-254del	ENSP00000263431.3:n.-254del
ENST00000419486.1:c.-441del	ENSP00000387919.2:n.-441del
ENST00000474397.5:c.-322-316del	ENSP00000471271.1:n.-322-316del
ENST00000479081.5:c.-322-316del	ENSP00000471544.1:n.-322-316del
NM_001316329.1:c.-254del	NP_001303258.1:n.-254del
NM_002739.3:c.-254del , LRG_669t1:c.-254del	NP_002730.1:n.-254del
NM_002739.4:c.-254del	NP_002730.1:n.-254del
NM_002739.5:c.-254del MANE Select	NP_002730.1:n.-254del
NM_001316329.2:c.-254del	NP_001303258.1:n.-254del