Canonical Allele Identifier: CA633905585

Gene: PRKCG

Linked Data

• dbSNP Id: rs1165222736
• gnomAD v2: 19-54385550-TC-T
• gnomAD v4: 19-53882296-TC-T
• MyVariant Identifiers: chr19:g.54385551del (hg19) ; chr19:g.53882297del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882301del , CM000681.2:g.53882301del	GRCh38
NC_000019.9:g.54385555del , CM000681.1:g.54385555del	GRCh37
NC_000019.8:g.59077367del	NCBI36
NG_009114.1:g.5089del , LRG_669:g.5089del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-194del	ENSP00000507230.1:n.-194del
ENST00000682268.1:n.105del
ENST00000682902.1:n.109del
ENST00000683513.1:c.-194del	ENSP00000506809.1:n.-194del
ENST00000263431.4:c.-194del MANE Select	ENSP00000263431.3:n.-194del
ENST00000263431.3:c.-194del	ENSP00000263431.3:n.-194del
ENST00000419486.1:c.-381del	ENSP00000387919.2:n.-381del
ENST00000474397.5:c.-322-256del	ENSP00000471271.1:n.-322-256del
ENST00000479081.5:c.-322-256del	ENSP00000471544.1:n.-322-256del
NM_001316329.1:c.-194del	NP_001303258.1:n.-194del
NM_002739.3:c.-194del , LRG_669t1:c.-194del	NP_002730.1:n.-194del
NM_002739.4:c.-194del	NP_002730.1:n.-194del
NM_002739.5:c.-194del MANE Select	NP_002730.1:n.-194del
NM_001316329.2:c.-194del	NP_001303258.1:n.-194del