Canonical Allele Identifier: CA9640302

Gene: PRKCG

Linked Data

• dbSNP Id: rs752281737
• ExAC: 19:54393249 A / G
• gnomAD v2: 19-54393249-A-G
• gnomAD v3: 19-53889995-A-G
• gnomAD v4: 19-53889995-A-G
• MyVariant Identifiers: chr19:g.54393249A>G (hg19) ; chr19:g.53889995A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889995A>G , CM000681.2:g.53889995A>G	GRCh38
NC_000019.9:g.54393249A>G , CM000681.1:g.54393249A>G	GRCh37
NC_000019.8:g.59085061A>G	NCBI36
NG_009114.1:g.12783A>G , LRG_669:g.12783A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.507A>G	ENSP00000507230.1:p.Thr169=
ENST00000682268.1:n.805A>G
ENST00000682902.1:n.809A>G
ENST00000683513.1:c.507A>G	ENSP00000506809.1:p.Thr169=
ENST00000263431.4:c.507A>G MANE Select	ENSP00000263431.3:p.Thr169=
ENST00000263431.3:c.507A>G	ENSP00000263431.3:p.Thr169=
ENST00000474397.5:c.123A>G	ENSP00000471271.1:p.Thr41=
NM_001316329.1:c.507A>G	NP_001303258.1:p.Thr169=
NM_002739.3:c.507A>G , LRG_669t1:c.507A>G	NP_002730.1:p.Thr169=
NM_002739.4:c.507A>G	NP_002730.1:p.Thr169=
NM_002739.5:c.507A>G MANE Select	NP_002730.1:p.Thr169=
NM_001316329.2:c.507A>G	NP_001303258.1:p.Thr169=