Canonical Allele Identifier: CA2814830472
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882256dup , CM000681.2:g.53882256dup GRCh38
NC_000019.9:g.54385510dup , CM000681.1:g.54385510dup GRCh37
NC_000019.8:g.59077322dup NCBI36
NG_009114.1:g.5044dup , LRG_669:g.5044dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-239dup ENSP00000507230.1:n.-239dup
ENST00000682268.1:n.60dup
ENST00000682902.1:n.64dup
ENST00000683513.1:c.-239dup ENSP00000506809.1:n.-239dup
ENST00000263431.4:c.-239dup MANE Select ENSP00000263431.3:n.-239dup
ENST00000263431.3:c.-239dup ENSP00000263431.3:n.-239dup
ENST00000419486.1:c.-426dup ENSP00000387919.2:n.-426dup
ENST00000474397.5:c.-322-301dup ENSP00000471271.1:n.-322-301dup
ENST00000479081.5:c.-322-301dup ENSP00000471544.1:n.-322-301dup
NM_001316329.1:c.-239dup NP_001303258.1:n.-239dup
NM_002739.3:c.-239dup , LRG_669t1:c.-239dup NP_002730.1:n.-239dup
NM_002739.4:c.-239dup NP_002730.1:n.-239dup
NM_002739.5:c.-239dup MANE Select NP_002730.1:n.-239dup
NM_001316329.2:c.-239dup NP_001303258.1:n.-239dup