Canonical Allele Identifier: CA633905568

Gene: PRKCG

Linked Data

• dbSNP Id: rs1439988519
• gnomAD v2: 19-54385508-GC-G
• gnomAD v4: 19-53882254-GC-G
• MyVariant Identifiers: chr19:g.54385509del (hg19) ; chr19:g.53882255del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53882256del , CM000681.2:g.53882256del	GRCh38
NC_000019.9:g.54385510del , CM000681.1:g.54385510del	GRCh37
NC_000019.8:g.59077322del	NCBI36
NG_009114.1:g.5044del , LRG_669:g.5044del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.-239del	ENSP00000507230.1:n.-239del
ENST00000682268.1:n.60del
ENST00000682902.1:n.64del
ENST00000683513.1:c.-239del	ENSP00000506809.1:n.-239del
ENST00000263431.4:c.-239del MANE Select	ENSP00000263431.3:n.-239del
ENST00000263431.3:c.-239del	ENSP00000263431.3:n.-239del
ENST00000419486.1:c.-426del	ENSP00000387919.2:n.-426del
ENST00000474397.5:c.-322-301del	ENSP00000471271.1:n.-322-301del
ENST00000479081.5:c.-322-301del	ENSP00000471544.1:n.-322-301del
NM_001316329.1:c.-239del	NP_001303258.1:n.-239del
NM_002739.3:c.-239del , LRG_669t1:c.-239del	NP_002730.1:n.-239del
NM_002739.4:c.-239del	NP_002730.1:n.-239del
NM_002739.5:c.-239del MANE Select	NP_002730.1:n.-239del
NM_001316329.2:c.-239del	NP_001303258.1:n.-239del