Canonical Allele Identifier: CA2586975114

Gene: PRKCG

Linked Data

• gnomAD v4: 19-53900861-GTGGCCTTCTTACACAGCCAGTCGTTCCTCCAGCCTCCAGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900862_53900902del , CM000681.2:g.53900862_53900902del	GRCh38
NC_000019.9:g.54404116_54404156del , CM000681.1:g.54404116_54404156del	GRCh37
NC_000019.8:g.59095928_59095968del	NCBI36
NG_009114.1:g.23650_23690del , LRG_669:g.23650_23690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+113_1575+153del	ENSP00000507230.1:n.1575+113_1575+153del
ENST00000682268.1:n.1873+113_1873+153del
ENST00000682676.1:n.976+113_976+153del
ENST00000682902.1:n.1877+113_1877+153del
ENST00000683513.1:c.1575+113_1575+153del	ENSP00000506809.1:n.1575+113_1575+153del
ENST00000263431.4:c.1575+113_1575+153del MANE Select	ENSP00000263431.3:n.1575+113_1575+153del
ENST00000263431.3:c.1575+113_1575+153del	ENSP00000263431.3:n.1575+113_1575+153del
NM_001316329.1:c.1575+113_1575+153del	NP_001303258.1:n.1575+113_1575+153del
NM_002739.3:c.1575+113_1575+153del , LRG_669t1:c.1575+113_1575+153del	NP_002730.1:n.1575+113_1575+153del
NM_002739.4:c.1575+113_1575+153del	NP_002730.1:n.1575+113_1575+153del
XM_011527108.1:c.666+113_666+153del	XP_011525410.1:n.666+113_666+153del
NM_002739.5:c.1575+113_1575+153del MANE Select	NP_002730.1:n.1575+113_1575+153del
NM_001316329.2:c.1575+113_1575+153del	NP_001303258.1:n.1575+113_1575+153del