Canonical Allele Identifier: CA2586962396

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53882293-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882293C>A , CM000681.2:g.53882293C>A	GRCh38
NC_000019.9:g.54385547C>A , CM000681.1:g.54385547C>A	GRCh37
NC_000019.8:g.59077359C>A	NCBI36
NG_009114.1:g.5081C>A , LRG_669:g.5081C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-202C>A	ENSP00000507230.1:n.-202C>A
ENST00000682268.1:n.97C>A
ENST00000682902.1:n.101C>A
ENST00000683513.1:c.-202C>A	ENSP00000506809.1:n.-202C>A
ENST00000263431.4:c.-202C>A MANE Select	ENSP00000263431.3:n.-202C>A
ENST00000263431.3:c.-202C>A	ENSP00000263431.3:n.-202C>A
ENST00000419486.1:c.-389C>A	ENSP00000387919.2:n.-389C>A
ENST00000474397.5:c.-322-264C>A	ENSP00000471271.1:n.-322-264C>A
ENST00000479081.5:c.-322-264C>A	ENSP00000471544.1:n.-322-264C>A
NM_001316329.1:c.-202C>A	NP_001303258.1:n.-202C>A
NM_002739.3:c.-202C>A , LRG_669t1:c.-202C>A	NP_002730.1:n.-202C>A
NM_002739.4:c.-202C>A	NP_002730.1:n.-202C>A
NM_002739.5:c.-202C>A MANE Select	NP_002730.1:n.-202C>A
NM_001316329.2:c.-202C>A	NP_001303258.1:n.-202C>A