Canonical Allele Identifier: CA1547396565
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232957C= , CM000667.2:g.55232957C= GRCh38
NC_000005.9:g.54528785C= , CM000667.1:g.54528785C= GRCh37
NC_000005.8:g.54564542C= NCBI36
NG_034201.1:g.5761G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+186G= MANE Select ENSP00000282572.4:n.381+186G=
ENST00000282572.4:c.381+186G= ENSP00000282572.4:n.381+186G=
ENST00000501463.2:c.*171G= ENSP00000422485.1:n.*171G=
NM_021147.4:c.381+186G= NP_066970.3:n.381+186G=
NR_125346.1:n.761G=
NR_125347.1:n.580+181G=
NR_125348.1:n.35G=
NM_021147.5:c.381+186G= MANE Select NP_066970.3:n.381+186G=
NR_125346.2:n.652G=
NR_125347.2:n.471+181G=
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