Canonical Allele Identifier: CA2673856337
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232962-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232966del , CM000667.2:g.55232966del GRCh38
NC_000005.9:g.54528794del , CM000667.1:g.54528794del GRCh37
NC_000005.8:g.54564551del NCBI36
NG_034201.1:g.5755del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+180del MANE Select ENSP00000282572.4:n.381+180del
ENST00000282572.4:c.381+180del ENSP00000282572.4:n.381+180del
ENST00000501463.2:c.*165del ENSP00000422485.1:n.*165del
NM_021147.4:c.381+180del NP_066970.3:n.381+180del
NR_125346.1:n.755del
NR_125347.1:n.580+175del
NR_125348.1:n.29del
NM_021147.5:c.381+180del MANE Select NP_066970.3:n.381+180del
NR_125346.2:n.646del
NR_125347.2:n.471+175del
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Search 100 bp 3'