Canonical Allele Identifier: CA1139666579

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 994943
• ClinVar RCV Id: RCV001288725
• dbSNP Id: rs2068657289

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889714_53889731dup , CM000681.2:g.53889714_53889731dup	GRCh38
NC_000019.9:g.54392968_54392985dup , CM000681.1:g.54392968_54392985dup	GRCh37
NC_000019.8:g.59084780_59084797dup	NCBI36
NG_009114.1:g.12502_12519dup , LRG_669:g.12502_12519dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000682028.1:c.362_379dup	ENSP00000507230.1:p.His126_Gln127insLeuTy...
ENST00000682268.1:n.660_677dup
ENST00000682902.1:n.664_681dup
ENST00000683513.1:c.362_379dup	ENSP00000506809.1:p.His126_Gln127insLeuTy...
ENST00000263431.4:c.362_379dup MANE Select	ENSP00000263431.3:p.His126_Gln127insLeuTy...
ENST00000263431.3:c.362_379dup	ENSP00000263431.3:p.His126_Gln127insLeuTy...
ENST00000419486.1:c.-23_-6dup	ENSP00000387919.2:n.-23_-6dup
ENST00000474397.5:c.-23_-6dup	ENSP00000471271.1:n.-23_-6dup
ENST00000479081.5:c.-23_-6dup	ENSP00000471544.1:n.-23_-6dup
NM_001316329.1:c.362_379dup	NP_001303258.1:p.His126_Gln127insLeuTyrGl...
NM_002739.3:c.362_379dup , LRG_669t1:c.362_379dup	NP_002730.1:p.His126_Gln127insLeuTyrGlyLe...
NM_002739.4:c.362_379dup	NP_002730.1:p.His126_Gln127insLeuTyrGlyLe...
NM_002739.5:c.362_379dup MANE Select	NP_002730.1:p.His126_Gln127insLeuTyrGlyLe...
NM_001316329.2:c.362_379dup	NP_001303258.1:p.His126_Gln127insLeuTyrGl...