Canonical Allele Identifier: CA2586962393
Gene: PRKCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882300_53882334del , CM000681.2:g.53882300_53882334del GRCh38
NC_000019.9:g.54385554_54385588del , CM000681.1:g.54385554_54385588del GRCh37
NC_000019.8:g.59077366_59077400del NCBI36
NG_009114.1:g.5088_5122del , LRG_669:g.5088_5122del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-195_-161del ENSP00000507230.1:n.-195_-161del
ENST00000682268.1:n.104_138del
ENST00000682902.1:n.108_142del
ENST00000683513.1:c.-195_-161del ENSP00000506809.1:n.-195_-161del
ENST00000263431.4:c.-195_-161del MANE Select ENSP00000263431.3:n.-195_-161del
ENST00000263431.3:c.-195_-161del ENSP00000263431.3:n.-195_-161del
ENST00000419486.1:c.-382_-348del ENSP00000387919.2:n.-382_-348del
ENST00000474397.5:c.-322-257_-322-223del ENSP00000471271.1:n.-322-257_-322-223del
ENST00000479081.5:c.-322-257_-322-223del ENSP00000471544.1:n.-322-257_-322-223del
NM_001316329.1:c.-195_-161del NP_001303258.1:n.-195_-161del
NM_002739.3:c.-195_-161del , LRG_669t1:c.-195_-161del NP_002730.1:n.-195_-161del
NM_002739.4:c.-195_-161del NP_002730.1:n.-195_-161del
NM_002739.5:c.-195_-161del MANE Select NP_002730.1:n.-195_-161del
NM_001316329.2:c.-195_-161del NP_001303258.1:n.-195_-161del