Canonical Allele Identifier: CA2586962358

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53882268-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882271dup , CM000681.2:g.53882271dup	GRCh38
NC_000019.9:g.54385525dup , CM000681.1:g.54385525dup	GRCh37
NC_000019.8:g.59077337dup	NCBI36
NG_009114.1:g.5059dup , LRG_669:g.5059dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-224dup	ENSP00000507230.1:n.-224dup
ENST00000682268.1:n.75dup
ENST00000682902.1:n.79dup
ENST00000683513.1:c.-224dup	ENSP00000506809.1:n.-224dup
ENST00000263431.4:c.-224dup MANE Select	ENSP00000263431.3:n.-224dup
ENST00000263431.3:c.-224dup	ENSP00000263431.3:n.-224dup
ENST00000419486.1:c.-411dup	ENSP00000387919.2:n.-411dup
ENST00000474397.5:c.-322-286dup	ENSP00000471271.1:n.-322-286dup
ENST00000479081.5:c.-322-286dup	ENSP00000471544.1:n.-322-286dup
NM_001316329.1:c.-224dup	NP_001303258.1:n.-224dup
NM_002739.3:c.-224dup , LRG_669t1:c.-224dup	NP_002730.1:n.-224dup
NM_002739.4:c.-224dup	NP_002730.1:n.-224dup
NM_002739.5:c.-224dup MANE Select	NP_002730.1:n.-224dup
NM_001316329.2:c.-224dup	NP_001303258.1:n.-224dup