Canonical Allele Identifier: CA1547396657
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233111G= , CM000667.2:g.55233111G= GRCh38
NC_000005.9:g.54528939G= , CM000667.1:g.54528939G= GRCh37
NC_000005.8:g.54564696G= NCBI36
NG_034201.1:g.5607C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+32C= MANE Select ENSP00000282572.4:n.381+32C=
ENST00000282572.4:c.381+32C= ENSP00000282572.4:n.381+32C=
ENST00000501463.2:c.*17C= ENSP00000422485.1:n.*17C=
NM_021147.4:c.381+32C= NP_066970.3:n.381+32C=
NR_125346.1:n.607C=
NR_125347.1:n.580+27C=
NM_021147.5:c.381+32C= MANE Select NP_066970.3:n.381+32C=
NR_125346.2:n.498C=
NR_125347.2:n.471+27C=
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