Canonical Allele Identifier: CA407414283

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 1027509
• ClinVar RCV Id: RCV001647231
• dbSNP Id: rs121918515
• MyVariant Identifiers: chr19:g.54392986A>C (hg19) ; chr19:g.53889732A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889732A>C , CM000681.2:g.53889732A>C	GRCh38
NC_000019.9:g.54392986A>C , CM000681.1:g.54392986A>C	GRCh37
NC_000019.8:g.59084798A>C	NCBI36
NG_009114.1:g.12520A>C , LRG_669:g.12520A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682028.1:c.380A>C	ENSP00000507230.1:p.Gln127Pro
ENST00000682268.1:n.678A>C
ENST00000682902.1:n.682A>C
ENST00000683513.1:c.380A>C	ENSP00000506809.1:p.Gln127Pro
ENST00000263431.4:c.380A>C MANE Select	ENSP00000263431.3:p.Gln127Pro
ENST00000263431.3:c.380A>C	ENSP00000263431.3:p.Gln127Pro
ENST00000419486.1:c.-5A>C	ENSP00000387919.2:n.-5A>C
ENST00000474397.5:c.-5A>C	ENSP00000471271.1:n.-5A>C
ENST00000479081.5:c.-5A>C	ENSP00000471544.1:n.-5A>C
NM_001316329.1:c.380A>C	NP_001303258.1:p.Gln127Pro
NM_002739.3:c.380A>C , LRG_669t1:c.380A>C	NP_002730.1:p.Gln127Pro
NM_002739.4:c.380A>C	NP_002730.1:p.Gln127Pro
NM_002739.5:c.380A>C MANE Select	NP_002730.1:p.Gln127Pro
NM_001316329.2:c.380A>C	NP_001303258.1:p.Gln127Pro