Canonical Allele Identifier: CA1547390894
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1745667905
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233511del , CM000667.2:g.55233511del GRCh38
NC_000005.9:g.54529339del , CM000667.1:g.54529339del GRCh37
NC_000005.8:g.54565096del NCBI36
NG_034201.1:g.5207del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.13del MANE Select ENSP00000282572.4:p.Cys5ValfsTer25
ENST00000282572.4:c.13del ENSP00000282572.4:p.Cys5ValfsTer25
ENST00000501463.2:c.13del ENSP00000422485.1:p.Cys5ValfsTer25
NM_021147.4:c.13del NP_066970.3:p.Cys5ValfsTer25
NR_125346.1:n.207del
NR_125347.1:n.207del
NM_021147.5:c.13del MANE Select NP_066970.3:p.Cys5ValfsTer25
NR_125346.2:n.98del
NR_125347.2:n.98del
Search 100 bp 5'
Search 100 bp 3'