Canonical Allele Identifier: CA1547396606
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233041G= , CM000667.2:g.55233041G= GRCh38
NC_000005.9:g.54528869G= , CM000667.1:g.54528869G= GRCh37
NC_000005.8:g.54564626G= NCBI36
NG_034201.1:g.5677C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+102C= MANE Select ENSP00000282572.4:n.381+102C=
ENST00000282572.4:c.381+102C= ENSP00000282572.4:n.381+102C=
ENST00000501463.2:c.*87C= ENSP00000422485.1:n.*87C=
NM_021147.4:c.381+102C= NP_066970.3:n.381+102C=
NR_125346.1:n.677C=
NR_125347.1:n.580+97C=
NM_021147.5:c.381+102C= MANE Select NP_066970.3:n.381+102C=
NR_125346.2:n.568C=
NR_125347.2:n.471+97C=
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