Canonical Allele Identifier: CA2342584787
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900623G= , CM000681.2:g.53900623G= GRCh38
NC_000019.9:g.54403877G= , CM000681.1:g.54403877G= GRCh37
NC_000019.8:g.59095689G= NCBI36
NG_009114.1:g.23411G= , LRG_669:g.23411G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.1449G= ENSP00000507230.1:p.Leu483=
ENST00000682268.1:n.1747G=
ENST00000682676.1:n.850G=
ENST00000682902.1:n.1751G=
ENST00000683513.1:c.1449G= ENSP00000506809.1:p.Leu483=
ENST00000263431.4:c.1449G= MANE Select ENSP00000263431.3:p.Leu483=
ENST00000263431.3:c.1449G= ENSP00000263431.3:p.Leu483=
NM_001316329.1:c.1449G= NP_001303258.1:p.Leu483=
NM_002739.3:c.1449G= , LRG_669t1:c.1449G= NP_002730.1:p.Leu483=
NM_002739.4:c.1449G= NP_002730.1:p.Leu483=
XM_011527108.1:c.540G= XP_011525410.1:p.Leu180=
NM_002739.5:c.1449G= MANE Select NP_002730.1:p.Leu483=
NM_001316329.2:c.1449G= NP_001303258.1:p.Leu483=