Canonical Allele Identifier: CA2342579523
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53890147A= , CM000681.2:g.53890147A= GRCh38
NC_000019.9:g.54393401A= , CM000681.1:g.54393401A= GRCh37
NC_000019.8:g.59085213A= NCBI36
NG_009114.1:g.12935A= , LRG_669:g.12935A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.529+130A= ENSP00000507230.1:n.529+130A=
ENST00000682268.1:n.827+130A=
ENST00000682902.1:n.831+130A=
ENST00000683513.1:c.529+130A= ENSP00000506809.1:n.529+130A=
ENST00000263431.4:c.529+130A= MANE Select ENSP00000263431.3:n.529+130A=
ENST00000263431.3:c.529+130A= ENSP00000263431.3:n.529+130A=
ENST00000474397.5:c.145+130A= ENSP00000471271.1:n.145+130A=
NM_001316329.1:c.529+130A= NP_001303258.1:n.529+130A=
NM_002739.3:c.529+130A= , LRG_669t1:c.529+130A= NP_002730.1:n.529+130A=
NM_002739.4:c.529+130A= NP_002730.1:n.529+130A=
NM_002739.5:c.529+130A= MANE Select NP_002730.1:n.529+130A=
NM_001316329.2:c.529+130A= NP_001303258.1:n.529+130A=