Canonical Allele Identifier: CA14741055
Gene: PRKCG HGNC NCBI

Linked Data

ClinVar Variation Id: 1270032
ClinVar RCV Id: RCV001684190
dbSNP Id: rs2242245

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53900547T>C , CM000681.2:g.53900547T>C GRCh38
NC_000019.9:g.54403801T>C , CM000681.1:g.54403801T>C GRCh37
NC_000019.8:g.59095613T>C NCBI36
NG_009114.1:g.23335T>C , LRG_669:g.23335T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682028.1:c.1437-64T>C ENSP00000507230.1:n.1437-64T>C
ENST00000682268.1:n.1735-64T>C
ENST00000682676.1:n.838-64T>C
ENST00000682902.1:n.1739-64T>C
ENST00000683513.1:c.1437-64T>C ENSP00000506809.1:n.1437-64T>C
ENST00000263431.4:c.1437-64T>C MANE Select ENSP00000263431.3:n.1437-64T>C
ENST00000263431.3:c.1437-64T>C ENSP00000263431.3:n.1437-64T>C
NM_001316329.1:c.1437-64T>C NP_001303258.1:n.1437-64T>C
NM_002739.3:c.1437-64T>C , LRG_669t1:c.1437-64T>C NP_002730.1:n.1437-64T>C
NM_002739.4:c.1437-64T>C NP_002730.1:n.1437-64T>C
XM_011527108.1:c.528-64T>C XP_011525410.1:n.528-64T>C
NM_002739.5:c.1437-64T>C MANE Select NP_002730.1:n.1437-64T>C
NM_001316329.2:c.1437-64T>C NP_001303258.1:n.1437-64T>C