Canonical Allele Identifier: CA2342584923

Gene: PRKCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.53900987_53900988delinsTC , CM000681.2:g.53900987_53900988delinsTC	GRCh38
NC_000019.9:g.54404241_54404242delinsTC , CM000681.1:g.54404241_54404242delinsTC	GRCh37
NC_000019.8:g.59096053_59096054delinsTC	NCBI36
NG_009114.1:g.23775_23776delinsTC , LRG_669:g.23775_23776delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682028.1:c.1575+238_1575+239delinsTC	ENSP00000507230.1:n.1575+238_1575+239delinsTC
ENST00000682268.1:n.1873+238_1873+239delinsTC
ENST00000682676.1:n.976+238_976+239delinsTC
ENST00000682902.1:n.1877+238_1877+239delinsTC
ENST00000683513.1:c.1575+238_1575+239delinsTC	ENSP00000506809.1:n.1575+238_1575+239delinsTC
ENST00000263431.4:c.1575+238_1575+239delinsTC MANE Select	ENSP00000263431.3:n.1575+238_1575+239delinsTC
ENST00000263431.3:c.1575+238_1575+239delinsTC	ENSP00000263431.3:n.1575+238_1575+239delinsTC
NM_001316329.1:c.1575+238_1575+239delinsTC	NP_001303258.1:n.1575+238_1575+239delinsTC
NM_002739.3:c.1575+238_1575+239delinsTC , LRG_669t1:c.1575+238_1575+239delinsTC	NP_002730.1:n.1575+238_1575+239delinsTC
NM_002739.4:c.1575+238_1575+239delinsTC	NP_002730.1:n.1575+238_1575+239delinsTC
XM_011527108.1:c.666+238_666+239delinsTC	XP_011525410.1:n.666+238_666+239delinsTC
NM_002739.5:c.1575+238_1575+239delinsTC MANE Select	NP_002730.1:n.1575+238_1575+239delinsTC
NM_001316329.2:c.1575+238_1575+239delinsTC	NP_001303258.1:n.1575+238_1575+239delinsTC