Canonical Allele Identifier: CA1547390966
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233584C= , CM000667.2:g.55233584C= GRCh38
NC_000005.9:g.54529412C= , CM000667.1:g.54529412C= GRCh37
NC_000005.8:g.54565169C= NCBI36
NG_034201.1:g.5134G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-61G= MANE Select ENSP00000282572.4:n.-61G=
ENST00000282572.4:c.-61G= ENSP00000282572.4:n.-61G=
ENST00000501463.2:c.-61G= ENSP00000422485.1:n.-61G=
NM_021147.4:c.-61G= NP_066970.3:n.-61G=
NR_125346.1:n.134G=
NR_125347.1:n.134G=
NM_021147.5:c.-61G= MANE Select NP_066970.3:n.-61G=
NR_125346.2:n.25G=
NR_125347.2:n.25G=
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