Canonical Allele Identifier: CA2673856885
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233591-GAA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233593_55233594del , CM000667.2:g.55233593_55233594del GRCh38
NC_000005.9:g.54529421_54529422del , CM000667.1:g.54529421_54529422del GRCh37
NC_000005.8:g.54565178_54565179del NCBI36
NG_034201.1:g.5125_5126del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-70_-69del MANE Select ENSP00000282572.4:n.-70_-69del
ENST00000282572.4:c.-70_-69del ENSP00000282572.4:n.-70_-69del
ENST00000501463.2:c.-70_-69del ENSP00000422485.1:n.-70_-69del
NM_021147.4:c.-70_-69del NP_066970.3:n.-70_-69del
NR_125346.1:n.125_126del
NR_125347.1:n.125_126del
NM_021147.5:c.-70_-69del MANE Select NP_066970.3:n.-70_-69del
NR_125346.2:n.16_17del
NR_125347.2:n.16_17del
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