Canonical Allele Identifier: CA2586975009

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900380-CACT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900381_53900383del , CM000681.2:g.53900381_53900383del	GRCh38
NC_000019.9:g.54403635_54403637del , CM000681.1:g.54403635_54403637del	GRCh37
NC_000019.8:g.59095447_59095449del	NCBI36
NG_009114.1:g.23169_23171del , LRG_669:g.23169_23171del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1374-38_1374-36del	ENSP00000507230.1:n.1374-38_1374-36del
ENST00000682268.1:n.1672-38_1672-36del
ENST00000682676.1:n.775-38_775-36del
ENST00000682902.1:n.1676-38_1676-36del
ENST00000683513.1:c.1374-38_1374-36del	ENSP00000506809.1:n.1374-38_1374-36del
ENST00000263431.4:c.1374-38_1374-36del MANE Select	ENSP00000263431.3:n.1374-38_1374-36del
ENST00000263431.3:c.1374-38_1374-36del	ENSP00000263431.3:n.1374-38_1374-36del
NM_001316329.1:c.1374-38_1374-36del	NP_001303258.1:n.1374-38_1374-36del
NM_002739.3:c.1374-38_1374-36del , LRG_669t1:c.1374-38_1374-36del	NP_002730.1:n.1374-38_1374-36del
NM_002739.4:c.1374-38_1374-36del	NP_002730.1:n.1374-38_1374-36del
XM_011527108.1:c.465-38_465-36del	XP_011525410.1:n.465-38_465-36del
NM_002739.5:c.1374-38_1374-36del MANE Select	NP_002730.1:n.1374-38_1374-36del
NM_001316329.2:c.1374-38_1374-36del	NP_001303258.1:n.1374-38_1374-36del