Canonical Allele Identifier: CA2342575868
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882357G= , CM000681.2:g.53882357G= GRCh38
NC_000019.9:g.54385611G= , CM000681.1:g.54385611G= GRCh37
NC_000019.8:g.59077423G= NCBI36
NG_009114.1:g.5145G= , LRG_669:g.5145G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-138G= ENSP00000507230.1:n.-138G=
ENST00000682268.1:n.161G=
ENST00000682902.1:n.165G=
ENST00000683513.1:c.-138G= ENSP00000506809.1:n.-138G=
ENST00000263431.4:c.-138G= MANE Select ENSP00000263431.3:n.-138G=
ENST00000263431.3:c.-138G= ENSP00000263431.3:n.-138G=
ENST00000419486.1:c.-325G= ENSP00000387919.2:n.-325G=
ENST00000474397.5:c.-322-200G= ENSP00000471271.1:n.-322-200G=
ENST00000479081.5:c.-322-200G= ENSP00000471544.1:n.-322-200G=
NM_001316329.1:c.-138G= NP_001303258.1:n.-138G=
NM_002739.3:c.-138G= , LRG_669t1:c.-138G= NP_002730.1:n.-138G=
NM_002739.4:c.-138G= NP_002730.1:n.-138G=
NM_002739.5:c.-138G= MANE Select NP_002730.1:n.-138G=
NM_001316329.2:c.-138G= NP_001303258.1:n.-138G=