Canonical Allele Identifier: CA1547396538
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232916T= , CM000667.2:g.55232916T= GRCh38
NC_000005.9:g.54528744T= , CM000667.1:g.54528744T= GRCh37
NC_000005.8:g.54564501T= NCBI36
NG_034201.1:g.5802A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+227A= MANE Select ENSP00000282572.4:n.381+227A=
ENST00000282572.4:c.381+227A= ENSP00000282572.4:n.381+227A=
ENST00000501463.2:c.*212A= ENSP00000422485.1:n.*212A=
NM_021147.4:c.381+227A= NP_066970.3:n.381+227A=
NR_125346.1:n.802A=
NR_125347.1:n.580+222A=
NR_125348.1:n.76A=
NM_021147.5:c.381+227A= MANE Select NP_066970.3:n.381+227A=
NR_125346.2:n.693A=
NR_125347.2:n.471+222A=
Search 100 bp 5'
Search 100 bp 3'