Canonical Allele Identifier: CA407414543

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53889982-T-A
• MyVariant Identifiers: chr19:g.54393236T>A (hg19) ; chr19:g.53889982T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889982T>A , CM000681.2:g.53889982T>A	GRCh38
NC_000019.9:g.54393236T>A , CM000681.1:g.54393236T>A	GRCh37
NC_000019.8:g.59085048T>A	NCBI36
NG_009114.1:g.12770T>A , LRG_669:g.12770T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.494T>A	ENSP00000507230.1:p.Ile165Asn
ENST00000682268.1:n.792T>A
ENST00000682902.1:n.796T>A
ENST00000683513.1:c.494T>A	ENSP00000506809.1:p.Ile165Asn
ENST00000263431.4:c.494T>A MANE Select	ENSP00000263431.3:p.Ile165Asn
ENST00000263431.3:c.494T>A	ENSP00000263431.3:p.Ile165Asn
ENST00000474397.5:c.110T>A	ENSP00000471271.1:p.Ile37Asn
NM_001316329.1:c.494T>A	NP_001303258.1:p.Ile165Asn
NM_002739.3:c.494T>A , LRG_669t1:c.494T>A	NP_002730.1:p.Ile165Asn
NM_002739.4:c.494T>A	NP_002730.1:p.Ile165Asn
NM_002739.5:c.494T>A MANE Select	NP_002730.1:p.Ile165Asn
NM_001316329.2:c.494T>A	NP_001303258.1:p.Ile165Asn