Canonical Allele Identifier: CA2766523762
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233291del , CM000667.2:g.55233291del GRCh38
NC_000005.9:g.54529119del , CM000667.1:g.54529119del GRCh37
NC_000005.8:g.54564876del NCBI36
NG_034201.1:g.5430del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.236del MANE Select ENSP00000282572.4:p.Gly79ValfsTer15
ENST00000282572.4:c.236del ENSP00000282572.4:p.Gly79ValfsTer15
ENST00000501463.2:c.236del ENSP00000422485.1:p.Gly79ValfsTer15
NM_021147.4:c.236del NP_066970.3:p.Gly79ValfsTer15
NR_125346.1:n.430del
NR_125347.1:n.430del
NM_021147.5:c.236del MANE Select NP_066970.3:p.Gly79ValfsTer15
NR_125346.2:n.321del
NR_125347.2:n.321del
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