Canonical Allele Identifier: CA2736011516

Gene: PRKCG

Linked Data

• dbSNP Id: rs2123017669

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900955del , CM000681.2:g.53900955del	GRCh38
NC_000019.9:g.54404209del , CM000681.1:g.54404209del	GRCh37
NC_000019.8:g.59096021del	NCBI36
NG_009114.1:g.23743del , LRG_669:g.23743del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+206del	ENSP00000507230.1:n.1575+206del
ENST00000682268.1:n.1873+206del
ENST00000682676.1:n.976+206del
ENST00000682902.1:n.1877+206del
ENST00000683513.1:c.1575+206del	ENSP00000506809.1:n.1575+206del
ENST00000263431.4:c.1575+206del MANE Select	ENSP00000263431.3:n.1575+206del
ENST00000263431.3:c.1575+206del	ENSP00000263431.3:n.1575+206del
NM_001316329.1:c.1575+206del	NP_001303258.1:n.1575+206del
NM_002739.3:c.1575+206del , LRG_669t1:c.1575+206del	NP_002730.1:n.1575+206del
NM_002739.4:c.1575+206del	NP_002730.1:n.1575+206del
XM_011527108.1:c.666+206del	XP_011525410.1:n.666+206del
NM_002739.5:c.1575+206del MANE Select	NP_002730.1:n.1575+206del
NM_001316329.2:c.1575+206del	NP_001303258.1:n.1575+206del