Canonical Allele Identifier: CA10649073
Gene: PRKCG HGNC NCBI

Linked Data

ClinVar Variation Id: 330079
ClinVar RCV Id: RCV000351941
dbSNP Id: rs886054615
gnomAD v2: 19-54410576-T-C
gnomAD v3: 19-53907322-T-C
gnomAD v4: 19-53907322-T-C
MyVariant Identifiers: chr19:g.54410576T>C (hg19) chr19:g.53907322T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53907322T>C , CM000681.2:g.53907322T>C GRCh38
NC_000019.9:g.54410576T>C , CM000681.1:g.54410576T>C GRCh37
NC_000019.8:g.59102388T>C NCBI36
NG_009114.1:g.30110T>C , LRG_669:g.30110T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.*286T>C ENSP00000507230.1:n.*286T>C
ENST00000682676.1:n.1922T>C
ENST00000263431.4:c.*427T>C MANE Select ENSP00000263431.3:n.*427T>C
ENST00000263431.3:c.*427T>C ENSP00000263431.3:n.*427T>C
NM_001316329.1:c.*286T>C NP_001303258.1:n.*286T>C
NM_002739.3:c.*427T>C , LRG_669t1:c.*427T>C NP_002730.1:n.*427T>C
NM_002739.4:c.*427T>C NP_002730.1:n.*427T>C
XM_011527108.1:c.*286T>C XP_011525410.1:n.*286T>C
NM_002739.5:c.*427T>C MANE Select NP_002730.1:n.*427T>C
NM_001316329.2:c.*286T>C NP_001303258.1:n.*286T>C
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