Canonical Allele Identifier: CA2342575863
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882349C= , CM000681.2:g.53882349C= GRCh38
NC_000019.9:g.54385603C= , CM000681.1:g.54385603C= GRCh37
NC_000019.8:g.59077415C= NCBI36
NG_009114.1:g.5137C= , LRG_669:g.5137C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-146C= ENSP00000507230.1:n.-146C=
ENST00000682268.1:n.153C=
ENST00000682902.1:n.157C=
ENST00000683513.1:c.-146C= ENSP00000506809.1:n.-146C=
ENST00000263431.4:c.-146C= MANE Select ENSP00000263431.3:n.-146C=
ENST00000263431.3:c.-146C= ENSP00000263431.3:n.-146C=
ENST00000419486.1:c.-333C= ENSP00000387919.2:n.-333C=
ENST00000474397.5:c.-322-208C= ENSP00000471271.1:n.-322-208C=
ENST00000479081.5:c.-322-208C= ENSP00000471544.1:n.-322-208C=
NM_001316329.1:c.-146C= NP_001303258.1:n.-146C=
NM_002739.3:c.-146C= , LRG_669t1:c.-146C= NP_002730.1:n.-146C=
NM_002739.4:c.-146C= NP_002730.1:n.-146C=
NM_002739.5:c.-146C= MANE Select NP_002730.1:n.-146C=
NM_001316329.2:c.-146C= NP_001303258.1:n.-146C=