Canonical Allele Identifier: CA2342584624
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900294A= , CM000681.2:g.53900294A= GRCh38
NC_000019.9:g.54403548A= , CM000681.1:g.54403548A= GRCh37
NC_000019.8:g.59095360A= NCBI36
NG_009114.1:g.23082A= , LRG_669:g.23082A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.1343A= ENSP00000507230.1:p.Gln448=
ENST00000682268.1:n.1641A=
ENST00000682676.1:n.744A=
ENST00000682902.1:n.1645A=
ENST00000683513.1:c.1343A= ENSP00000506809.1:p.Gln448=
ENST00000263431.4:c.1343A= MANE Select ENSP00000263431.3:p.Gln448=
ENST00000263431.3:c.1343A= ENSP00000263431.3:p.Gln448=
NM_001316329.1:c.1343A= NP_001303258.1:p.Gln448=
NM_002739.3:c.1343A= , LRG_669t1:c.1343A= NP_002730.1:p.Gln448=
NM_002739.4:c.1343A= NP_002730.1:p.Gln448=
XM_011527108.1:c.434A= XP_011525410.1:p.Gln145=
NM_002739.5:c.1343A= MANE Select NP_002730.1:p.Gln448=
NM_001316329.2:c.1343A= NP_001303258.1:p.Gln448=