Canonical Allele Identifier: CA2586975132

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900875-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900875_53900876insTT , CM000681.2:g.53900875_53900876insTT	GRCh38
NC_000019.9:g.54404129_54404130insTT , CM000681.1:g.54404129_54404130insTT	GRCh37
NC_000019.8:g.59095941_59095942insTT	NCBI36
NG_009114.1:g.23663_23664insTT , LRG_669:g.23663_23664insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+126_1575+127insTT	ENSP00000507230.1:n.1575+126_1575+127insTT
ENST00000682268.1:n.1873+126_1873+127insTT
ENST00000682676.1:n.976+126_976+127insTT
ENST00000682902.1:n.1877+126_1877+127insTT
ENST00000683513.1:c.1575+126_1575+127insTT	ENSP00000506809.1:n.1575+126_1575+127insTT
ENST00000263431.4:c.1575+126_1575+127insTT MANE Select	ENSP00000263431.3:n.1575+126_1575+127insTT
ENST00000263431.3:c.1575+126_1575+127insTT	ENSP00000263431.3:n.1575+126_1575+127insTT
NM_001316329.1:c.1575+126_1575+127insTT	NP_001303258.1:n.1575+126_1575+127insTT
NM_002739.3:c.1575+126_1575+127insTT , LRG_669t1:c.1575+126_1575+127insTT	NP_002730.1:n.1575+126_1575+127insTT
NM_002739.4:c.1575+126_1575+127insTT	NP_002730.1:n.1575+126_1575+127insTT
XM_011527108.1:c.666+126_666+127insTT	XP_011525410.1:n.666+126_666+127insTT
NM_002739.5:c.1575+126_1575+127insTT MANE Select	NP_002730.1:n.1575+126_1575+127insTT
NM_001316329.2:c.1575+126_1575+127insTT	NP_001303258.1:n.1575+126_1575+127insTT