Canonical Allele Identifier: CA2573054825

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 1314858
• ClinVar RCV Id: RCV001765899
• dbSNP Id: rs2122988509

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889693_53889708del , CM000681.2:g.53889693_53889708del	GRCh38
NC_000019.9:g.54392947_54392962del , CM000681.1:g.54392947_54392962del	GRCh37
NC_000019.8:g.59084759_59084774del	NCBI36
NG_009114.1:g.12481_12496del , LRG_669:g.12481_12496del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682028.1:c.341_356del	ENSP00000507230.1:p.Cys114SerfsTer11
ENST00000682268.1:n.639_654del
ENST00000682902.1:n.643_658del
ENST00000683513.1:c.341_356del	ENSP00000506809.1:p.Cys114SerfsTer11
ENST00000263431.4:c.341_356del MANE Select	ENSP00000263431.3:p.Cys114SerfsTer11
ENST00000263431.3:c.341_356del	ENSP00000263431.3:p.Cys114SerfsTer11
ENST00000419486.1:c.-44_-29del	ENSP00000387919.2:n.-44_-29del
ENST00000474397.5:c.-44_-29del	ENSP00000471271.1:n.-44_-29del
ENST00000479081.5:c.-44_-29del	ENSP00000471544.1:n.-44_-29del
NM_001316329.1:c.341_356del	NP_001303258.1:p.Cys114SerfsTer11
NM_002739.3:c.341_356del , LRG_669t1:c.341_356del	NP_002730.1:p.Cys114SerfsTer11
NM_002739.4:c.341_356del	NP_002730.1:p.Cys114SerfsTer11
NM_002739.5:c.341_356del MANE Select	NP_002730.1:p.Cys114SerfsTer11
NM_001316329.2:c.341_356del	NP_001303258.1:p.Cys114SerfsTer11