Canonical Allele Identifier: CA344618

Gene: PRKCG

Linked Data

• ClinVar Variation Id: 42157
• ClinVar RCV Id: RCV000034984
• dbSNP Id: rs386134161
• MyVariant Identifiers: chr19:g.54392902_54392907del (hg19) ; chr19:g.53889648_53889653del (hg38)
• PubMed: PMID:15824357 ; PMID:20301573

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53889652_53889657del , CM000681.2:g.53889652_53889657del	GRCh38
NC_000019.9:g.54392906_54392911del , CM000681.1:g.54392906_54392911del	GRCh37
NC_000019.8:g.59084718_59084723del	NCBI36
NG_009114.1:g.12440_12445del , LRG_669:g.12440_12445del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.300_305del	ENSP00000507230.1:p.His101_Lys102del
ENST00000682268.1:n.598_603del
ENST00000682902.1:n.602_607del
ENST00000683513.1:c.300_305del	ENSP00000506809.1:p.His101_Lys102del
ENST00000263431.4:c.300_305del MANE Select	ENSP00000263431.3:p.His101_Lys102del
ENST00000263431.3:c.300_305del	ENSP00000263431.3:p.His101_Lys102del
ENST00000419486.1:c.-85_-80del	ENSP00000387919.2:n.-85_-80del
ENST00000474397.5:c.-85_-80del	ENSP00000471271.1:n.-85_-80del
ENST00000479081.5:c.-85_-80del	ENSP00000471544.1:n.-85_-80del
NM_001316329.1:c.300_305del	NP_001303258.1:p.His101_Lys102del
NM_002739.3:c.300_305del , LRG_669t1:c.300_305del	NP_002730.1:p.His101_Lys102del
NM_002739.4:c.300_305del	NP_002730.1:p.His101_Lys102del
NM_002739.5:c.300_305del MANE Select	NP_002730.1:p.His101_Lys102del
NM_001316329.2:c.300_305del	NP_001303258.1:p.His101_Lys102del