Canonical Allele Identifier: CA2673856903
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233606-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233608del , CM000667.2:g.55233608del GRCh38
NC_000005.9:g.54529436del , CM000667.1:g.54529436del GRCh37
NC_000005.8:g.54565193del NCBI36
NG_034201.1:g.5111del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-84del MANE Select ENSP00000282572.4:n.-84del
ENST00000282572.4:c.-84del ENSP00000282572.4:n.-84del
NM_021147.4:c.-84del NP_066970.3:n.-84del
NR_125346.1:n.111del
NR_125347.1:n.111del
NM_021147.5:c.-84del MANE Select NP_066970.3:n.-84del
NR_125346.2:n.2del
NR_125347.2:n.2del
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