Canonical Allele Identifier: CA9640567
Gene: PRKCG HGNC NCBI

Linked Data

dbSNP Id: rs778623561

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.1343A>T ENSP00000507230.1:p.Gln448Leu
ENST00000682268.1:n.1641A>T
ENST00000682676.1:n.744A>T
ENST00000682902.1:n.1645A>T
ENST00000683513.1:c.1343A>T ENSP00000506809.1:p.Gln448Leu
ENST00000263431.4:c.1343A>T MANE Select ENSP00000263431.3:p.Gln448Leu
ENST00000263431.3:c.1343A>T ENSP00000263431.3:p.Gln448Leu
NM_001316329.1:c.1343A>T NP_001303258.1:p.Gln448Leu
NM_002739.3:c.1343A>T , LRG_669t1:c.1343A>T NP_002730.1:p.Gln448Leu
NM_002739.4:c.1343A>T NP_002730.1:p.Gln448Leu
XM_011527108.1:c.434A>T XP_011525410.1:p.Gln145Leu
NM_002739.5:c.1343A>T MANE Select NP_002730.1:p.Gln448Leu
NM_001316329.2:c.1343A>T NP_001303258.1:p.Gln448Leu