Canonical Allele Identifier: CA9640624

Gene: PRKCG

Linked Data

• dbSNP Id: rs772438019
• ExAC: 19:54403925 TG / T
• gnomAD v2: 19-54403925-TG-T
• MyVariant Identifiers: chr19:g.54403926del (hg19) ; chr19:g.53900672del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900673del , CM000681.2:g.53900673del	GRCh38
NC_000019.9:g.54403927del , CM000681.1:g.54403927del	GRCh37
NC_000019.8:g.59095739del	NCBI36
NG_009114.1:g.23461del , LRG_669:g.23461del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1499del	ENSP00000507230.1:p.Gly500AlafsTer23
ENST00000682268.1:n.1797del
ENST00000682676.1:n.900del
ENST00000682902.1:n.1801del
ENST00000683513.1:c.1499del	ENSP00000506809.1:p.Gly500AlafsTer23
ENST00000263431.4:c.1499del MANE Select	ENSP00000263431.3:p.Gly500AlafsTer23
ENST00000263431.3:c.1499del	ENSP00000263431.3:p.Gly500AlafsTer23
NM_001316329.1:c.1499del	NP_001303258.1:p.Gly500AlafsTer23
NM_002739.3:c.1499del , LRG_669t1:c.1499del	NP_002730.1:p.Gly500AlafsTer23
NM_002739.4:c.1499del	NP_002730.1:p.Gly500AlafsTer23
XM_011527108.1:c.590del	XP_011525410.1:p.Gly197AlafsTer23
NM_002739.5:c.1499del MANE Select	NP_002730.1:p.Gly500AlafsTer23
NM_001316329.2:c.1499del	NP_001303258.1:p.Gly500AlafsTer23