Canonical Allele Identifier: CA1547396591
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233011T= , CM000667.2:g.55233011T= GRCh38
NC_000005.9:g.54528839T= , CM000667.1:g.54528839T= GRCh37
NC_000005.8:g.54564596T= NCBI36
NG_034201.1:g.5707A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+132A= MANE Select ENSP00000282572.4:n.381+132A=
ENST00000282572.4:c.381+132A= ENSP00000282572.4:n.381+132A=
ENST00000501463.2:c.*117A= ENSP00000422485.1:n.*117A=
NM_021147.4:c.381+132A= NP_066970.3:n.381+132A=
NR_125346.1:n.707A=
NR_125347.1:n.580+127A=
NM_021147.5:c.381+132A= MANE Select NP_066970.3:n.381+132A=
NR_125346.2:n.598A=
NR_125347.2:n.471+127A=
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