Canonical Allele Identifier: CA2342579254
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53889656A= , CM000681.2:g.53889656A= GRCh38
NC_000019.9:g.54392910A= , CM000681.1:g.54392910A= GRCh37
NC_000019.8:g.59084722A= NCBI36
NG_009114.1:g.12444A= , LRG_669:g.12444A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.304A= ENSP00000507230.1:p.Lys102=
ENST00000682268.1:n.602A=
ENST00000682902.1:n.606A=
ENST00000683513.1:c.304A= ENSP00000506809.1:p.Lys102=
ENST00000263431.4:c.304A= MANE Select ENSP00000263431.3:p.Lys102=
ENST00000263431.3:c.304A= ENSP00000263431.3:p.Lys102=
ENST00000419486.1:c.-81A= ENSP00000387919.2:n.-81A=
ENST00000474397.5:c.-81A= ENSP00000471271.1:n.-81A=
ENST00000479081.5:c.-81A= ENSP00000471544.1:n.-81A=
NM_001316329.1:c.304A= NP_001303258.1:p.Lys102=
NM_002739.3:c.304A= , LRG_669t1:c.304A= NP_002730.1:p.Lys102=
NM_002739.4:c.304A= NP_002730.1:p.Lys102=
NM_002739.5:c.304A= MANE Select NP_002730.1:p.Lys102=
NM_001316329.2:c.304A= NP_001303258.1:p.Lys102=