Canonical Allele Identifier: CA344624

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 42163
• ClinVar RCV Id: RCV000034990 ; RCV000713005
• dbSNP Id: rs386134163
• MyVariant Identifiers: chr19:g.54392962C>T (hg19) ; chr19:g.53889708C>T (hg38)
• PubMed: PMID:16763984 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889708C>T , CM000681.2:g.53889708C>T	GRCh38
NC_000019.9:g.54392962C>T , CM000681.1:g.54392962C>T	GRCh37
NC_000019.8:g.59084774C>T	NCBI36
NG_009114.1:g.12496C>T , LRG_669:g.12496C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.356C>T	ENSP00000507230.1:p.Ser119Phe
ENST00000682268.1:n.654C>T
ENST00000682902.1:n.658C>T
ENST00000683513.1:c.356C>T	ENSP00000506809.1:p.Ser119Phe
ENST00000263431.4:c.356C>T MANE Select	ENSP00000263431.3:p.Ser119Phe
ENST00000263431.3:c.356C>T	ENSP00000263431.3:p.Ser119Phe
ENST00000419486.1:c.-29C>T	ENSP00000387919.2:n.-29C>T
ENST00000474397.5:c.-29C>T	ENSP00000471271.1:n.-29C>T
ENST00000479081.5:c.-29C>T	ENSP00000471544.1:n.-29C>T
NM_001316329.1:c.356C>T	NP_001303258.1:p.Ser119Phe
NM_002739.3:c.356C>T , LRG_669t1:c.356C>T	NP_002730.1:p.Ser119Phe
NM_002739.4:c.356C>T	NP_002730.1:p.Ser119Phe
NM_002739.5:c.356C>T MANE Select	NP_002730.1:p.Ser119Phe
NM_001316329.2:c.356C>T	NP_001303258.1:p.Ser119Phe