Canonical Allele Identifier: CA883512843

Gene: PRKCG

Linked Data

• dbSNP Id: rs771133027
• MyVariant Identifiers: chr19:g.54385653T>C (hg19) ; chr19:g.53882399T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882399T>C , CM000681.2:g.53882399T>C	GRCh38
NC_000019.9:g.54385653T>C , CM000681.1:g.54385653T>C	GRCh37
NC_000019.8:g.59077465T>C	NCBI36
NG_009114.1:g.5187T>C , LRG_669:g.5187T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-96T>C	ENSP00000507230.1:n.-96T>C
ENST00000682268.1:n.203T>C
ENST00000682902.1:n.207T>C
ENST00000683513.1:c.-96T>C	ENSP00000506809.1:n.-96T>C
ENST00000263431.4:c.-96T>C MANE Select	ENSP00000263431.3:n.-96T>C
ENST00000263431.3:c.-96T>C	ENSP00000263431.3:n.-96T>C
ENST00000419486.1:c.-323+40T>C	ENSP00000387919.2:n.-323+40T>C
ENST00000474397.5:c.-322-158T>C	ENSP00000471271.1:n.-322-158T>C
ENST00000479081.5:c.-322-158T>C	ENSP00000471544.1:n.-322-158T>C
NM_001316329.1:c.-96T>C	NP_001303258.1:n.-96T>C
NM_002739.3:c.-96T>C , LRG_669t1:c.-96T>C	NP_002730.1:n.-96T>C
NM_002739.4:c.-96T>C	NP_002730.1:n.-96T>C
NM_002739.5:c.-96T>C MANE Select	NP_002730.1:n.-96T>C
NM_001316329.2:c.-96T>C	NP_001303258.1:n.-96T>C