Canonical Allele Identifier: CA407414570

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53889997-C-T
• MyVariant Identifiers: chr19:g.54393251C>T (hg19) ; chr19:g.53889997C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889997C>T , CM000681.2:g.53889997C>T	GRCh38
NC_000019.9:g.54393251C>T , CM000681.1:g.54393251C>T	GRCh37
NC_000019.8:g.59085063C>T	NCBI36
NG_009114.1:g.12785C>T , LRG_669:g.12785C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.509C>T	ENSP00000507230.1:p.Ala170Val
ENST00000682268.1:n.807C>T
ENST00000682902.1:n.811C>T
ENST00000683513.1:c.509C>T	ENSP00000506809.1:p.Ala170Val
ENST00000263431.4:c.509C>T MANE Select	ENSP00000263431.3:p.Ala170Val
ENST00000263431.3:c.509C>T	ENSP00000263431.3:p.Ala170Val
ENST00000474397.5:c.125C>T	ENSP00000471271.1:p.Ala42Val
NM_001316329.1:c.509C>T	NP_001303258.1:p.Ala170Val
NM_002739.3:c.509C>T , LRG_669t1:c.509C>T	NP_002730.1:p.Ala170Val
NM_002739.4:c.509C>T	NP_002730.1:p.Ala170Val
NM_002739.5:c.509C>T MANE Select	NP_002730.1:p.Ala170Val
NM_001316329.2:c.509C>T	NP_001303258.1:p.Ala170Val