Canonical Allele Identifier: CA2342584674

Gene: PRKCG

Linked Data

• dbSNP Id: rs2068754120
• gnomAD v4: 19-53900378-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900380dup , CM000681.2:g.53900380dup	GRCh38
NC_000019.9:g.54403634dup , CM000681.1:g.54403634dup	GRCh37
NC_000019.8:g.59095446dup	NCBI36
NG_009114.1:g.23168dup , LRG_669:g.23168dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1374-39dup	ENSP00000507230.1:n.1374-39dup
ENST00000682268.1:n.1672-39dup
ENST00000682676.1:n.775-39dup
ENST00000682902.1:n.1676-39dup
ENST00000683513.1:c.1374-39dup	ENSP00000506809.1:n.1374-39dup
ENST00000263431.4:c.1374-39dup MANE Select	ENSP00000263431.3:n.1374-39dup
ENST00000263431.3:c.1374-39dup	ENSP00000263431.3:n.1374-39dup
NM_001316329.1:c.1374-39dup	NP_001303258.1:n.1374-39dup
NM_002739.3:c.1374-39dup , LRG_669t1:c.1374-39dup	NP_002730.1:n.1374-39dup
NM_002739.4:c.1374-39dup	NP_002730.1:n.1374-39dup
XM_011527108.1:c.465-39dup	XP_011525410.1:n.465-39dup
NM_002739.5:c.1374-39dup MANE Select	NP_002730.1:n.1374-39dup
NM_001316329.2:c.1374-39dup	NP_001303258.1:n.1374-39dup