Canonical Allele Identifier: CA407418427
Gene: PRKCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900323G>A , CM000681.2:g.53900323G>A GRCh38
NC_000019.9:g.54403577G>A , CM000681.1:g.54403577G>A GRCh37
NC_000019.8:g.59095389G>A NCBI36
NG_009114.1:g.23111G>A , LRG_669:g.23111G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.1372G>A ENSP00000507230.1:p.Ala458Thr
ENST00000682268.1:n.1670G>A
ENST00000682676.1:n.773G>A
ENST00000682902.1:n.1674G>A
ENST00000683513.1:c.1372G>A ENSP00000506809.1:p.Ala458Thr
ENST00000263431.4:c.1372G>A MANE Select ENSP00000263431.3:p.Ala458Thr
ENST00000263431.3:c.1372G>A ENSP00000263431.3:p.Ala458Thr
NM_001316329.1:c.1372G>A NP_001303258.1:p.Ala458Thr
NM_002739.3:c.1372G>A , LRG_669t1:c.1372G>A NP_002730.1:p.Ala458Thr
NM_002739.4:c.1372G>A NP_002730.1:p.Ala458Thr
XM_011527108.1:c.463G>A XP_011525410.1:p.Ala155Thr
NM_002739.5:c.1372G>A MANE Select NP_002730.1:p.Ala458Thr
NM_001316329.2:c.1372G>A NP_001303258.1:p.Ala458Thr