Canonical Allele Identifier: CA1547396602
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233036G= , CM000667.2:g.55233036G= GRCh38
NC_000005.9:g.54528864G= , CM000667.1:g.54528864G= GRCh37
NC_000005.8:g.54564621G= NCBI36
NG_034201.1:g.5682C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+107C= MANE Select ENSP00000282572.4:n.381+107C=
ENST00000282572.4:c.381+107C= ENSP00000282572.4:n.381+107C=
ENST00000501463.2:c.*92C= ENSP00000422485.1:n.*92C=
NM_021147.4:c.381+107C= NP_066970.3:n.381+107C=
NR_125346.1:n.682C=
NR_125347.1:n.580+102C=
NM_021147.5:c.381+107C= MANE Select NP_066970.3:n.381+107C=
NR_125346.2:n.573C=
NR_125347.2:n.471+102C=
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