Canonical Allele Identifier: CA2586975020
Gene: PRKCG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900403_53900404del , CM000681.2:g.53900403_53900404del GRCh38
NC_000019.9:g.54403657_54403658del , CM000681.1:g.54403657_54403658del GRCh37
NC_000019.8:g.59095469_59095470del NCBI36
NG_009114.1:g.23191_23192del , LRG_669:g.23191_23192del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682028.1:c.1374-16_1374-15del ENSP00000507230.1:n.1374-16_1374-15del
ENST00000682268.1:n.1672-16_1672-15del
ENST00000682676.1:n.775-16_775-15del
ENST00000682902.1:n.1676-16_1676-15del
ENST00000683513.1:c.1374-16_1374-15del ENSP00000506809.1:n.1374-16_1374-15del
ENST00000263431.4:c.1374-16_1374-15del MANE Select ENSP00000263431.3:n.1374-16_1374-15del
ENST00000263431.3:c.1374-16_1374-15del ENSP00000263431.3:n.1374-16_1374-15del
NM_001316329.1:c.1374-16_1374-15del NP_001303258.1:n.1374-16_1374-15del
NM_002739.3:c.1374-16_1374-15del , LRG_669t1:c.1374-16_1374-15del NP_002730.1:n.1374-16_1374-15del
NM_002739.4:c.1374-16_1374-15del NP_002730.1:n.1374-16_1374-15del
XM_011527108.1:c.465-16_465-15del XP_011525410.1:n.465-16_465-15del
NM_002739.5:c.1374-16_1374-15del MANE Select NP_002730.1:n.1374-16_1374-15del
NM_001316329.2:c.1374-16_1374-15del NP_001303258.1:n.1374-16_1374-15del