Canonical Allele Identifier: CA407414365

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 871358
• ClinVar RCV Id: RCV001091269
• dbSNP Id: rs2068659547
• MyVariant Identifiers: chr19:g.54393151A>T (hg19) ; chr19:g.53889897A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889897A>T , CM000681.2:g.53889897A>T	GRCh38
NC_000019.9:g.54393151A>T , CM000681.1:g.54393151A>T	GRCh37
NC_000019.8:g.59084963A>T	NCBI36
NG_009114.1:g.12685A>T , LRG_669:g.12685A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.409A>T	ENSP00000507230.1:p.Asn137Tyr
ENST00000682268.1:n.707A>T
ENST00000682902.1:n.711A>T
ENST00000683513.1:c.409A>T	ENSP00000506809.1:p.Asn137Tyr
ENST00000263431.4:c.409A>T MANE Select	ENSP00000263431.3:p.Asn137Tyr
ENST00000263431.3:c.409A>T	ENSP00000263431.3:p.Asn137Tyr
ENST00000419486.1:c.25A>T	ENSP00000387919.2:p.Asn9Tyr
ENST00000474397.5:c.25A>T	ENSP00000471271.1:p.Asn9Tyr
ENST00000479081.5:c.25A>T	ENSP00000471544.1:p.Asn9Tyr
NM_001316329.1:c.409A>T	NP_001303258.1:p.Asn137Tyr
NM_002739.3:c.409A>T , LRG_669t1:c.409A>T	NP_002730.1:p.Asn137Tyr
NM_002739.4:c.409A>T	NP_002730.1:p.Asn137Tyr
NM_002739.5:c.409A>T MANE Select	NP_002730.1:p.Asn137Tyr
NM_001316329.2:c.409A>T	NP_001303258.1:p.Asn137Tyr