Canonical Allele Identifier: CA407414537

Gene: PRKCG

Linked Data

• dbSNP Id: rs1469824304
• gnomAD v2: 19-54393233-A-T
• gnomAD v4: 19-53889979-A-T
• MyVariant Identifiers: chr19:g.54393233A>T (hg19) ; chr19:g.53889979A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889979A>T , CM000681.2:g.53889979A>T	GRCh38
NC_000019.9:g.54393233A>T , CM000681.1:g.54393233A>T	GRCh37
NC_000019.8:g.59085045A>T	NCBI36
NG_009114.1:g.12767A>T , LRG_669:g.12767A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.491A>T	ENSP00000507230.1:p.Glu164Val
ENST00000682268.1:n.789A>T
ENST00000682902.1:n.793A>T
ENST00000683513.1:c.491A>T	ENSP00000506809.1:p.Glu164Val
ENST00000263431.4:c.491A>T MANE Select	ENSP00000263431.3:p.Glu164Val
ENST00000263431.3:c.491A>T	ENSP00000263431.3:p.Glu164Val
ENST00000419486.1:c.107A>T
ENST00000474397.5:c.107A>T	ENSP00000471271.1:p.Glu36Val
NM_001316329.1:c.491A>T	NP_001303258.1:p.Glu164Val
NM_002739.3:c.491A>T , LRG_669t1:c.491A>T	NP_002730.1:p.Glu164Val
NM_002739.4:c.491A>T	NP_002730.1:p.Glu164Val
NM_002739.5:c.491A>T MANE Select	NP_002730.1:p.Glu164Val
NM_001316329.2:c.491A>T	NP_001303258.1:p.Glu164Val