Canonical Allele Identifier: CA2830535930
Gene: PRKCI HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.170275445_170275457del , CM000665.2:g.170275445_170275457del GRCh38
NC_000003.11:g.169993233_169993245del , CM000665.1:g.169993233_169993245del GRCh37
NC_000003.10:g.171475927_171475939del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295797.5:c.705+158_705+170del MANE Select ENSP00000295797.4:n.705+158_705+170del
ENST00000295797.4:c.705+158_705+170del ENSP00000295797.4:n.705+158_705+170del
NM_002740.5:c.705+158_705+170del NP_002731.4:n.705+158_705+170del
XM_017006860.1:c.309+158_309+170del XP_016862349.1:n.309+158_309+170del
XR_001740206.1:n.870+158_870+170del
NM_002740.6:c.705+158_705+170del MANE Select NP_002731.4:n.705+158_705+170del