Canonical Allele Identifier: CA2586963277

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53889625-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889625T>C , CM000681.2:g.53889625T>C	GRCh38
NC_000019.9:g.54392879T>C , CM000681.1:g.54392879T>C	GRCh37
NC_000019.8:g.59084691T>C	NCBI36
NG_009114.1:g.12413T>C , LRG_669:g.12413T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682028.1:c.286-13T>C	ENSP00000507230.1:n.286-13T>C
ENST00000682268.1:n.584-13T>C
ENST00000682902.1:n.588-13T>C
ENST00000683513.1:c.286-13T>C	ENSP00000506809.1:n.286-13T>C
ENST00000263431.4:c.286-13T>C MANE Select	ENSP00000263431.3:n.286-13T>C
ENST00000263431.3:c.286-13T>C	ENSP00000263431.3:n.286-13T>C
ENST00000419486.1:c.-99-13T>C	ENSP00000387919.2:n.-99-13T>C
ENST00000474397.5:c.-99-13T>C	ENSP00000471271.1:n.-99-13T>C
ENST00000479081.5:c.-99-13T>C	ENSP00000471544.1:n.-99-13T>C
NM_001316329.1:c.286-13T>C	NP_001303258.1:n.286-13T>C
NM_002739.3:c.286-13T>C , LRG_669t1:c.286-13T>C	NP_002730.1:n.286-13T>C
NM_002739.4:c.286-13T>C	NP_002730.1:n.286-13T>C
NM_002739.5:c.286-13T>C MANE Select	NP_002730.1:n.286-13T>C
NM_001316329.2:c.286-13T>C	NP_001303258.1:n.286-13T>C