Canonical Allele Identifier: CA2586962348
Gene: PRKCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882265_53882300del , CM000681.2:g.53882265_53882300del GRCh38
NC_000019.9:g.54385519_54385554del , CM000681.1:g.54385519_54385554del GRCh37
NC_000019.8:g.59077331_59077366del NCBI36
NG_009114.1:g.5053_5088del , LRG_669:g.5053_5088del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-230_-195del ENSP00000507230.1:n.-230_-195del
ENST00000682268.1:n.69_104del
ENST00000682902.1:n.73_108del
ENST00000683513.1:c.-230_-195del ENSP00000506809.1:n.-230_-195del
ENST00000263431.4:c.-230_-195del MANE Select ENSP00000263431.3:n.-230_-195del
ENST00000263431.3:c.-230_-195del ENSP00000263431.3:n.-230_-195del
ENST00000419486.1:c.-417_-382del ENSP00000387919.2:n.-417_-382del
ENST00000474397.5:c.-322-292_-322-257del ENSP00000471271.1:n.-322-292_-322-257del
ENST00000479081.5:c.-322-292_-322-257del ENSP00000471544.1:n.-322-292_-322-257del
NM_001316329.1:c.-230_-195del NP_001303258.1:n.-230_-195del
NM_002739.3:c.-230_-195del , LRG_669t1:c.-230_-195del NP_002730.1:n.-230_-195del
NM_002739.4:c.-230_-195del NP_002730.1:n.-230_-195del
NM_002739.5:c.-230_-195del MANE Select NP_002730.1:n.-230_-195del
NM_001316329.2:c.-230_-195del NP_001303258.1:n.-230_-195del