Canonical Allele Identifier: CA1547396571
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232973C= , CM000667.2:g.55232973C= GRCh38
NC_000005.9:g.54528801C= , CM000667.1:g.54528801C= GRCh37
NC_000005.8:g.54564558C= NCBI36
NG_034201.1:g.5745G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+170G= MANE Select ENSP00000282572.4:n.381+170G=
ENST00000282572.4:c.381+170G= ENSP00000282572.4:n.381+170G=
ENST00000501463.2:c.*155G= ENSP00000422485.1:n.*155G=
NM_021147.4:c.381+170G= NP_066970.3:n.381+170G=
NR_125346.1:n.745G=
NR_125347.1:n.580+165G=
NR_125348.1:n.19G=
NM_021147.5:c.381+170G= MANE Select NP_066970.3:n.381+170G=
NR_125346.2:n.636G=
NR_125347.2:n.471+165G=
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