Canonical Allele Identifier: CA407411811
Gene: PRKCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882550T>C , CM000681.2:g.53882550T>C GRCh38
NC_000019.9:g.54385804T>C , CM000681.1:g.54385804T>C GRCh37
NC_000019.8:g.59077616T>C NCBI36
NG_009114.1:g.5338T>C , LRG_669:g.5338T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.56T>C ENSP00000507230.1:p.Phe19Ser
ENST00000682268.1:n.354T>C
ENST00000682902.1:n.358T>C
ENST00000683513.1:c.56T>C ENSP00000506809.1:p.Phe19Ser
ENST00000263431.4:c.56T>C MANE Select ENSP00000263431.3:p.Phe19Ser
ENST00000263431.3:c.56T>C ENSP00000263431.3:p.Phe19Ser
ENST00000419486.1:c.-322-7T>C ENSP00000387919.2:n.-322-7T>C
ENST00000474397.5:c.-322-7T>C ENSP00000471271.1:n.-322-7T>C
ENST00000479081.5:c.-322-7T>C ENSP00000471544.1:n.-322-7T>C
NM_001316329.1:c.56T>C NP_001303258.1:p.Phe19Ser
NM_002739.3:c.56T>C , LRG_669t1:c.56T>C NP_002730.1:p.Phe19Ser
NM_002739.4:c.56T>C NP_002730.1:p.Phe19Ser
NM_002739.5:c.56T>C MANE Select NP_002730.1:p.Phe19Ser
NM_001316329.2:c.56T>C NP_001303258.1:p.Phe19Ser