Canonical Allele Identifier: CA1547396563
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232953T= , CM000667.2:g.55232953T= GRCh38
NC_000005.9:g.54528781T= , CM000667.1:g.54528781T= GRCh37
NC_000005.8:g.54564538T= NCBI36
NG_034201.1:g.5765A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+190A= MANE Select ENSP00000282572.4:n.381+190A=
ENST00000282572.4:c.381+190A= ENSP00000282572.4:n.381+190A=
ENST00000501463.2:c.*175A= ENSP00000422485.1:n.*175A=
NM_021147.4:c.381+190A= NP_066970.3:n.381+190A=
NR_125346.1:n.765A=
NR_125347.1:n.580+185A=
NR_125348.1:n.39A=
NM_021147.5:c.381+190A= MANE Select NP_066970.3:n.381+190A=
NR_125346.2:n.656A=
NR_125347.2:n.471+185A=
Search 100 bp 5'
Search 100 bp 3'