Canonical Allele Identifier: CA2576907861
Gene: PRKCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900567C>G , CM000681.2:g.53900567C>G GRCh38
NC_000019.9:g.54403821C>G , CM000681.1:g.54403821C>G GRCh37
NC_000019.8:g.59095633C>G NCBI36
NG_009114.1:g.23355C>G , LRG_669:g.23355C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.1437-44C>G ENSP00000507230.1:n.1437-44C>G
ENST00000682268.1:n.1735-44C>G
ENST00000682676.1:n.838-44C>G
ENST00000682902.1:n.1739-44C>G
ENST00000683513.1:c.1437-44C>G ENSP00000506809.1:n.1437-44C>G
ENST00000263431.4:c.1437-44C>G MANE Select ENSP00000263431.3:n.1437-44C>G
ENST00000263431.3:c.1437-44C>G ENSP00000263431.3:n.1437-44C>G
NM_001316329.1:c.1437-44C>G NP_001303258.1:n.1437-44C>G
NM_002739.3:c.1437-44C>G , LRG_669t1:c.1437-44C>G NP_002730.1:n.1437-44C>G
NM_002739.4:c.1437-44C>G NP_002730.1:n.1437-44C>G
XM_011527108.1:c.528-44C>G XP_011525410.1:n.528-44C>G
NM_002739.5:c.1437-44C>G MANE Select NP_002730.1:n.1437-44C>G
NM_001316329.2:c.1437-44C>G NP_001303258.1:n.1437-44C>G