Canonical Allele Identifier: CA920135593

Gene: PRKCG

Linked Data

• dbSNP Id: rs1599952156

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53901004_53901029del , CM000681.2:g.53901004_53901029del	GRCh38
NC_000019.9:g.54404258_54404283del , CM000681.1:g.54404258_54404283del	GRCh37
NC_000019.8:g.59096070_59096095del	NCBI36
NG_009114.1:g.23792_23817del , LRG_669:g.23792_23817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+255_1575+280del	ENSP00000507230.1:n.1575+255_1575+280del
ENST00000682268.1:n.1873+255_1873+280del
ENST00000682676.1:n.976+255_976+280del
ENST00000682902.1:n.1877+255_1877+280del
ENST00000683513.1:c.1575+255_1575+280del	ENSP00000506809.1:n.1575+255_1575+280del
ENST00000263431.4:c.1575+255_1575+280del MANE Select	ENSP00000263431.3:n.1575+255_1575+280del
ENST00000263431.3:c.1575+255_1575+280del	ENSP00000263431.3:n.1575+255_1575+280del
NM_001316329.1:c.1575+255_1575+280del	NP_001303258.1:n.1575+255_1575+280del
NM_002739.3:c.1575+255_1575+280del , LRG_669t1:c.1575+255_1575+280del	NP_002730.1:n.1575+255_1575+280del
NM_002739.4:c.1575+255_1575+280del	NP_002730.1:n.1575+255_1575+280del
XM_011527108.1:c.666+255_666+280del	XP_011525410.1:n.666+255_666+280del
NM_002739.5:c.1575+255_1575+280del MANE Select	NP_002730.1:n.1575+255_1575+280del
NM_001316329.2:c.1575+255_1575+280del	NP_001303258.1:n.1575+255_1575+280del