Canonical Allele Identifier: CA2342575906
Gene: PRKCG HGNC NCBI

Linked Data

dbSNP Id: rs2068599270

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882421_53882427del , CM000681.2:g.53882421_53882427del GRCh38
NC_000019.9:g.54385675_54385681del , CM000681.1:g.54385675_54385681del GRCh37
NC_000019.8:g.59077487_59077493del NCBI36
NG_009114.1:g.5209_5215del , LRG_669:g.5209_5215del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-74_-68del ENSP00000507230.1:n.-74_-68del
ENST00000682268.1:n.225_231del
ENST00000682902.1:n.229_235del
ENST00000683513.1:c.-74_-68del ENSP00000506809.1:n.-74_-68del
ENST00000263431.4:c.-74_-68del MANE Select ENSP00000263431.3:n.-74_-68del
ENST00000263431.3:c.-74_-68del ENSP00000263431.3:n.-74_-68del
ENST00000419486.1:c.-323+62_-323+68del ENSP00000387919.2:n.-323+62_-323+68del
ENST00000474397.5:c.-322-136_-322-130del ENSP00000471271.1:n.-322-136_-322-130del
ENST00000479081.5:c.-322-136_-322-130del ENSP00000471544.1:n.-322-136_-322-130del
NM_001316329.1:c.-74_-68del NP_001303258.1:n.-74_-68del
NM_002739.3:c.-74_-68del , LRG_669t1:c.-74_-68del NP_002730.1:n.-74_-68del
NM_002739.4:c.-74_-68del NP_002730.1:n.-74_-68del
NM_002739.5:c.-74_-68del MANE Select NP_002730.1:n.-74_-68del
NM_001316329.2:c.-74_-68del NP_001303258.1:n.-74_-68del