Canonical Allele Identifier: CA2342584702
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900427C= , CM000681.2:g.53900427C= GRCh38
NC_000019.9:g.54403681C= , CM000681.1:g.54403681C= GRCh37
NC_000019.8:g.59095493C= NCBI36
NG_009114.1:g.23215C= , LRG_669:g.23215C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.1382C= ENSP00000507230.1:p.Ala461=
ENST00000682268.1:n.1680C=
ENST00000682676.1:n.783C=
ENST00000682902.1:n.1684C=
ENST00000683513.1:c.1382C= ENSP00000506809.1:p.Ala461=
ENST00000263431.4:c.1382C= MANE Select ENSP00000263431.3:p.Ala461=
ENST00000263431.3:c.1382C= ENSP00000263431.3:p.Ala461=
NM_001316329.1:c.1382C= NP_001303258.1:p.Ala461=
NM_002739.3:c.1382C= , LRG_669t1:c.1382C= NP_002730.1:p.Ala461=
NM_002739.4:c.1382C= NP_002730.1:p.Ala461=
XM_011527108.1:c.473C= XP_011525410.1:p.Ala158=
NM_002739.5:c.1382C= MANE Select NP_002730.1:p.Ala461=
NM_001316329.2:c.1382C= NP_001303258.1:p.Ala461=