Canonical Allele Identifier: CA2342584895

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900918_53900920delinsCTG , CM000681.2:g.53900918_53900920delinsCTG	GRCh38
NC_000019.9:g.54404172_54404174delinsCTG , CM000681.1:g.54404172_54404174delinsCTG	GRCh37
NC_000019.8:g.59095984_59095986delinsCTG	NCBI36
NG_009114.1:g.23706_23708delinsCTG , LRG_669:g.23706_23708delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+169_1575+171delinsCTG	ENSP00000507230.1:n.1575+169_1575+171delinsCTG
ENST00000682268.1:n.1873+169_1873+171delinsCTG
ENST00000682676.1:n.976+169_976+171delinsCTG
ENST00000682902.1:n.1877+169_1877+171delinsCTG
ENST00000683513.1:c.1575+169_1575+171delinsCTG	ENSP00000506809.1:n.1575+169_1575+171delinsCTG
ENST00000263431.4:c.1575+169_1575+171delinsCTG MANE Select	ENSP00000263431.3:n.1575+169_1575+171delinsCTG
ENST00000263431.3:c.1575+169_1575+171delinsCTG	ENSP00000263431.3:n.1575+169_1575+171delinsCTG
NM_001316329.1:c.1575+169_1575+171delinsCTG	NP_001303258.1:n.1575+169_1575+171delinsCTG
NM_002739.3:c.1575+169_1575+171delinsCTG , LRG_669t1:c.1575+169_1575+171delinsCTG	NP_002730.1:n.1575+169_1575+171delinsCTG
NM_002739.4:c.1575+169_1575+171delinsCTG	NP_002730.1:n.1575+169_1575+171delinsCTG
XM_011527108.1:c.666+169_666+171delinsCTG	XP_011525410.1:n.666+169_666+171delinsCTG
NM_002739.5:c.1575+169_1575+171delinsCTG MANE Select	NP_002730.1:n.1575+169_1575+171delinsCTG
NM_001316329.2:c.1575+169_1575+171delinsCTG	NP_001303258.1:n.1575+169_1575+171delinsCTG