Canonical Allele Identifier: CA2586975122

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900865-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900869_53900871del , CM000681.2:g.53900869_53900871del	GRCh38
NC_000019.9:g.54404123_54404125del , CM000681.1:g.54404123_54404125del	GRCh37
NC_000019.8:g.59095935_59095937del	NCBI36
NG_009114.1:g.23657_23659del , LRG_669:g.23657_23659del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+120_1575+122del	ENSP00000507230.1:n.1575+120_1575+122del
ENST00000682268.1:n.1873+120_1873+122del
ENST00000682676.1:n.976+120_976+122del
ENST00000682902.1:n.1877+120_1877+122del
ENST00000683513.1:c.1575+120_1575+122del	ENSP00000506809.1:n.1575+120_1575+122del
ENST00000263431.4:c.1575+120_1575+122del MANE Select	ENSP00000263431.3:n.1575+120_1575+122del
ENST00000263431.3:c.1575+120_1575+122del	ENSP00000263431.3:n.1575+120_1575+122del
NM_001316329.1:c.1575+120_1575+122del	NP_001303258.1:n.1575+120_1575+122del
NM_002739.3:c.1575+120_1575+122del , LRG_669t1:c.1575+120_1575+122del	NP_002730.1:n.1575+120_1575+122del
NM_002739.4:c.1575+120_1575+122del	NP_002730.1:n.1575+120_1575+122del
XM_011527108.1:c.666+120_666+122del	XP_011525410.1:n.666+120_666+122del
NM_002739.5:c.1575+120_1575+122del MANE Select	NP_002730.1:n.1575+120_1575+122del
NM_001316329.2:c.1575+120_1575+122del	NP_001303258.1:n.1575+120_1575+122del