Canonical Allele Identifier: CA2342579432
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53890008C= , CM000681.2:g.53890008C= GRCh38
NC_000019.9:g.54393262C= , CM000681.1:g.54393262C= GRCh37
NC_000019.8:g.59085074C= NCBI36
NG_009114.1:g.12796C= , LRG_669:g.12796C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.520C= ENSP00000507230.1:p.His174=
ENST00000682268.1:n.818C=
ENST00000682902.1:n.822C=
ENST00000683513.1:c.520C= ENSP00000506809.1:p.His174=
ENST00000263431.4:c.520C= MANE Select ENSP00000263431.3:p.His174=
ENST00000263431.3:c.520C= ENSP00000263431.3:p.His174=
ENST00000474397.5:c.136C= ENSP00000471271.1:p.His46=
NM_001316329.1:c.520C= NP_001303258.1:p.His174=
NM_002739.3:c.520C= , LRG_669t1:c.520C= NP_002730.1:p.His174=
NM_002739.4:c.520C= NP_002730.1:p.His174=
NM_002739.5:c.520C= MANE Select NP_002730.1:p.His174=
NM_001316329.2:c.520C= NP_001303258.1:p.His174=