Canonical Allele Identifier: CA1547396570
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232972T= , CM000667.2:g.55232972T= GRCh38
NC_000005.9:g.54528800T= , CM000667.1:g.54528800T= GRCh37
NC_000005.8:g.54564557T= NCBI36
NG_034201.1:g.5746A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+171A= MANE Select ENSP00000282572.4:n.381+171A=
ENST00000282572.4:c.381+171A= ENSP00000282572.4:n.381+171A=
ENST00000501463.2:c.*156A= ENSP00000422485.1:n.*156A=
NM_021147.4:c.381+171A= NP_066970.3:n.381+171A=
NR_125346.1:n.746A=
NR_125347.1:n.580+166A=
NR_125348.1:n.20A=
NM_021147.5:c.381+171A= MANE Select NP_066970.3:n.381+171A=
NR_125346.2:n.637A=
NR_125347.2:n.471+166A=
Search 100 bp 5'
Search 100 bp 3'