Canonical Allele Identifier: CA2342584786
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900617G= , CM000681.2:g.53900617G= GRCh38
NC_000019.9:g.54403871G= , CM000681.1:g.54403871G= GRCh37
NC_000019.8:g.59095683G= NCBI36
NG_009114.1:g.23405G= , LRG_669:g.23405G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.1443G= ENSP00000507230.1:p.Leu481=
ENST00000682268.1:n.1741G=
ENST00000682676.1:n.844G=
ENST00000682902.1:n.1745G=
ENST00000683513.1:c.1443G= ENSP00000506809.1:p.Leu481=
ENST00000263431.4:c.1443G= MANE Select ENSP00000263431.3:p.Leu481=
ENST00000263431.3:c.1443G= ENSP00000263431.3:p.Leu481=
NM_001316329.1:c.1443G= NP_001303258.1:p.Leu481=
NM_002739.3:c.1443G= , LRG_669t1:c.1443G= NP_002730.1:p.Leu481=
NM_002739.4:c.1443G= NP_002730.1:p.Leu481=
XM_011527108.1:c.534G= XP_011525410.1:p.Leu178=
NM_002739.5:c.1443G= MANE Select NP_002730.1:p.Leu481=
NM_001316329.2:c.1443G= NP_001303258.1:p.Leu481=