Canonical Allele Identifier: CA2814830479
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882564dup , CM000681.2:g.53882564dup GRCh38
NC_000019.9:g.54385818dup , CM000681.1:g.54385818dup GRCh37
NC_000019.8:g.59077630dup NCBI36
NG_009114.1:g.5352dup , LRG_669:g.5352dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.70dup ENSP00000507230.1:p.Ala24GlyfsTer?
ENST00000682268.1:n.368dup
ENST00000682902.1:n.372dup
ENST00000683513.1:c.70dup ENSP00000506809.1:p.Ala24GlyfsTer?
ENST00000263431.4:c.70dup MANE Select ENSP00000263431.3:p.Ala24GlyfsTer?
ENST00000263431.3:c.70dup ENSP00000263431.3:p.Ala24GlyfsTer?
ENST00000419486.1:c.-315dup ENSP00000387919.2:n.-315dup
ENST00000474397.5:c.-315dup ENSP00000471271.1:n.-315dup
ENST00000479081.5:c.-315dup ENSP00000471544.1:n.-315dup
NM_001316329.1:c.70dup NP_001303258.1:p.Ala24GlyfsTer?
NM_002739.3:c.70dup , LRG_669t1:c.70dup NP_002730.1:p.Ala24GlyfsTer?
NM_002739.4:c.70dup NP_002730.1:p.Ala24GlyfsTer?
NM_002739.5:c.70dup MANE Select NP_002730.1:p.Ala24GlyfsTer?
NM_001316329.2:c.70dup NP_001303258.1:p.Ala24GlyfsTer?