Canonical Allele Identifier: CA1547396572
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232977A= , CM000667.2:g.55232977A= GRCh38
NC_000005.9:g.54528805A= , CM000667.1:g.54528805A= GRCh37
NC_000005.8:g.54564562A= NCBI36
NG_034201.1:g.5741T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+166T= MANE Select ENSP00000282572.4:n.381+166T=
ENST00000282572.4:c.381+166T= ENSP00000282572.4:n.381+166T=
ENST00000501463.2:c.*151T= ENSP00000422485.1:n.*151T=
NM_021147.4:c.381+166T= NP_066970.3:n.381+166T=
NR_125346.1:n.741T=
NR_125347.1:n.580+161T=
NR_125348.1:n.15T=
NM_021147.5:c.381+166T= MANE Select NP_066970.3:n.381+166T=
NR_125346.2:n.632T=
NR_125347.2:n.471+161T=
Search 100 bp 5'
Search 100 bp 3'