Canonical Allele Identifier: CA2842061963
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233308dup , CM000667.2:g.55233308dup GRCh38
NC_000005.9:g.54529136dup , CM000667.1:g.54529136dup GRCh37
NC_000005.8:g.54564893dup NCBI36
NG_034201.1:g.5410dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.216dup MANE Select ENSP00000282572.4:p.Ser73GlufsTer9
ENST00000282572.4:c.216dup ENSP00000282572.4:p.Ser73GlufsTer9
ENST00000501463.2:c.216dup ENSP00000422485.1:p.Ser73GlufsTer9
NM_021147.4:c.216dup NP_066970.3:p.Ser73GlufsTer9
NR_125346.1:n.410dup
NR_125347.1:n.410dup
NM_021147.5:c.216dup MANE Select NP_066970.3:p.Ser73GlufsTer9
NR_125346.2:n.301dup
NR_125347.2:n.301dup
Search 100 bp 5'
Search 100 bp 3'