Canonical Allele Identifier: CA2342575764
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882231_53882253delinsCGCCGCCGCCCGTGCCTCCGGCT , CM000681.2:g.53882231_53882253delinsCGCCGCCGCCCGTGCCTCCGGCT GRCh38
NC_000019.9:g.54385485_54385507delinsCGCCGCCGCCCGTGCCTCCGGCT , CM000681.1:g.54385485_54385507delinsCGCCGCCGCCCGTGCCTCCGGCT GRCh37
NC_000019.8:g.59077297_59077319delinsCGCCGCCGCCCGTGCCTCCGGCT NCBI36
NG_009114.1:g.5019_5041delinsCGCCGCCGCCCGTGCCTCCGGCT , LRG_669:g.5019_5041delinsCGCCGCCGCCCGTGCCTCCGGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT ENSP00000507230.1:n.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT
ENST00000682268.1:n.35_57delinsCGCCGCCGCCCGTGCCTCCGGCT
ENST00000682902.1:n.39_61delinsCGCCGCCGCCCGTGCCTCCGGCT
ENST00000683513.1:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT ENSP00000506809.1:n.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT
ENST00000263431.4:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT MANE Select ENSP00000263431.3:n.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT
ENST00000263431.3:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT ENSP00000263431.3:n.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT
ENST00000419486.1:c.-451_-429delinsCGCCGCCGCCCGTGCCTCCGGCT ENSP00000387919.2:n.-451_-429delinsCGCCGCCGCCCGTGCCTCCGGCT
ENST00000474397.5:c.-322-326_-322-304delinsCGCCGCCGCCCGTGCCTCCGGCT ENSP00000471271.1:n.-322-326_-322-304delinsCGCCGCCGCCCGTGCCTC...
ENST00000479081.5:c.-322-326_-322-304delinsCGCCGCCGCCCGTGCCTCCGGCT ENSP00000471544.1:n.-322-326_-322-304delinsCGCCGCCGCCCGTGCCTC...
NM_001316329.1:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT NP_001303258.1:n.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT
NM_002739.3:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT , LRG_669t1:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT NP_002730.1:n.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT
NM_002739.4:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT NP_002730.1:n.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT
NM_002739.5:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT MANE Select NP_002730.1:n.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT
NM_001316329.2:c.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT NP_001303258.1:n.-264_-242delinsCGCCGCCGCCCGTGCCTCCGGCT