Canonical Allele Identifier: CA2673856670
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233198del , CM000667.2:g.55233198del GRCh38
NC_000005.9:g.54529026del , CM000667.1:g.54529026del GRCh37
NC_000005.8:g.54564783del NCBI36
NG_034201.1:g.5520del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.326del MANE Select ENSP00000282572.4:p.Arg109ProfsTer20
ENST00000282572.4:c.326del ENSP00000282572.4:p.Arg109ProfsTer20
ENST00000501463.2:c.326del ENSP00000422485.1:p.Arg109ProfsTer20
NM_021147.4:c.326del NP_066970.3:p.Arg109ProfsTer20
NR_125346.1:n.520del
NR_125347.1:n.520del
NM_021147.5:c.326del MANE Select NP_066970.3:p.Arg109ProfsTer20
NR_125346.2:n.411del
NR_125347.2:n.411del