Canonical Allele Identifier: CA2586974958

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900153-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900155_53900156del , CM000681.2:g.53900155_53900156del	GRCh38
NC_000019.9:g.54403409_54403410del , CM000681.1:g.54403409_54403410del	GRCh37
NC_000019.8:g.59095221_59095222del	NCBI36
NG_009114.1:g.22943_22944del , LRG_669:g.22943_22944del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1282-78_1282-77del	ENSP00000507230.1:n.1282-78_1282-77del
ENST00000682268.1:n.1580-78_1580-77del
ENST00000682676.1:n.683-78_683-77del
ENST00000682902.1:n.1584-78_1584-77del
ENST00000683513.1:c.1282-78_1282-77del	ENSP00000506809.1:n.1282-78_1282-77del
ENST00000263431.4:c.1282-78_1282-77del MANE Select	ENSP00000263431.3:n.1282-78_1282-77del
ENST00000263431.3:c.1282-78_1282-77del	ENSP00000263431.3:n.1282-78_1282-77del
NM_001316329.1:c.1282-78_1282-77del	NP_001303258.1:n.1282-78_1282-77del
NM_002739.3:c.1282-78_1282-77del , LRG_669t1:c.1282-78_1282-77del	NP_002730.1:n.1282-78_1282-77del
NM_002739.4:c.1282-78_1282-77del	NP_002730.1:n.1282-78_1282-77del
XM_011527108.1:c.373-78_373-77del	XP_011525410.1:n.373-78_373-77del
NM_002739.5:c.1282-78_1282-77del MANE Select	NP_002730.1:n.1282-78_1282-77del
NM_001316329.2:c.1282-78_1282-77del	NP_001303258.1:n.1282-78_1282-77del