Canonical Allele Identifier: CA10643184

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 330084
• ClinVar RCV Id: RCV000299022
• dbSNP Id: rs186000310
• gnomAD v2: 19-54410819-T-C
• gnomAD v3: 19-53907565-T-C
• gnomAD v4: 19-53907565-T-C
• MyVariant Identifiers: chr19:g.54410819T>C (hg19) ; chr19:g.53907565T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53907565T>C , CM000681.2:g.53907565T>C	GRCh38
NC_000019.9:g.54410819T>C , CM000681.1:g.54410819T>C	GRCh37
NC_000019.8:g.59102631T>C	NCBI36
NG_009114.1:g.30353T>C , LRG_669:g.30353T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.*529T>C	ENSP00000507230.1:n.*529T>C
ENST00000682676.1:n.2165T>C
ENST00000263431.4:c.*670T>C MANE Select	ENSP00000263431.3:n.*670T>C
ENST00000263431.3:c.*670T>C	ENSP00000263431.3:n.*670T>C
NM_001316329.1:c.*529T>C	NP_001303258.1:n.*529T>C
NM_002739.3:c.*670T>C , LRG_669t1:c.*670T>C	NP_002730.1:n.*670T>C
NM_002739.4:c.*670T>C	NP_002730.1:n.*670T>C
XM_011527108.1:c.*529T>C	XP_011525410.1:n.*529T>C
NM_002739.5:c.*670T>C MANE Select	NP_002730.1:n.*670T>C
NM_001316329.2:c.*529T>C	NP_001303258.1:n.*529T>C