Canonical Allele Identifier: CA2586962378
Gene: PRKCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53882285del , CM000681.2:g.53882285del GRCh38
NC_000019.9:g.54385539del , CM000681.1:g.54385539del GRCh37
NC_000019.8:g.59077351del NCBI36
NG_009114.1:g.5073del , LRG_669:g.5073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.-210del ENSP00000507230.1:n.-210del
ENST00000682268.1:n.89del
ENST00000682902.1:n.93del
ENST00000683513.1:c.-210del ENSP00000506809.1:n.-210del
ENST00000263431.4:c.-210del MANE Select ENSP00000263431.3:n.-210del
ENST00000263431.3:c.-210del ENSP00000263431.3:n.-210del
ENST00000419486.1:c.-397del ENSP00000387919.2:n.-397del
ENST00000474397.5:c.-322-272del ENSP00000471271.1:n.-322-272del
ENST00000479081.5:c.-322-272del ENSP00000471544.1:n.-322-272del
NM_001316329.1:c.-210del NP_001303258.1:n.-210del
NM_002739.3:c.-210del , LRG_669t1:c.-210del NP_002730.1:n.-210del
NM_002739.4:c.-210del NP_002730.1:n.-210del
NM_002739.5:c.-210del MANE Select NP_002730.1:n.-210del
NM_001316329.2:c.-210del NP_001303258.1:n.-210del