Canonical Allele Identifier: CA1547396573
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232978A= , CM000667.2:g.55232978A= GRCh38
NC_000005.9:g.54528806A= , CM000667.1:g.54528806A= GRCh37
NC_000005.8:g.54564563A= NCBI36
NG_034201.1:g.5740T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+165T= MANE Select ENSP00000282572.4:n.381+165T=
ENST00000282572.4:c.381+165T= ENSP00000282572.4:n.381+165T=
ENST00000501463.2:c.*150T= ENSP00000422485.1:n.*150T=
NM_021147.4:c.381+165T= NP_066970.3:n.381+165T=
NR_125346.1:n.740T=
NR_125347.1:n.580+160T=
NR_125348.1:n.14T=
NM_021147.5:c.381+165T= MANE Select NP_066970.3:n.381+165T=
NR_125346.2:n.631T=
NR_125347.2:n.471+160T=
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