Canonical Allele Identifier: CA2586975092

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900838-ACCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900839_53900841del , CM000681.2:g.53900839_53900841del	GRCh38
NC_000019.9:g.54404093_54404095del , CM000681.1:g.54404093_54404095del	GRCh37
NC_000019.8:g.59095905_59095907del	NCBI36
NG_009114.1:g.23627_23629del , LRG_669:g.23627_23629del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+90_1575+92del	ENSP00000507230.1:n.1575+90_1575+92del
ENST00000682268.1:n.1873+90_1873+92del
ENST00000682676.1:n.976+90_976+92del
ENST00000682902.1:n.1877+90_1877+92del
ENST00000683513.1:c.1575+90_1575+92del	ENSP00000506809.1:n.1575+90_1575+92del
ENST00000263431.4:c.1575+90_1575+92del MANE Select	ENSP00000263431.3:n.1575+90_1575+92del
ENST00000263431.3:c.1575+90_1575+92del	ENSP00000263431.3:n.1575+90_1575+92del
NM_001316329.1:c.1575+90_1575+92del	NP_001303258.1:n.1575+90_1575+92del
NM_002739.3:c.1575+90_1575+92del , LRG_669t1:c.1575+90_1575+92del	NP_002730.1:n.1575+90_1575+92del
NM_002739.4:c.1575+90_1575+92del	NP_002730.1:n.1575+90_1575+92del
XM_011527108.1:c.666+90_666+92del	XP_011525410.1:n.666+90_666+92del
NM_002739.5:c.1575+90_1575+92del MANE Select	NP_002730.1:n.1575+90_1575+92del
NM_001316329.2:c.1575+90_1575+92del	NP_001303258.1:n.1575+90_1575+92del