Canonical Allele Identifier: CA1547390899
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233514G= , CM000667.2:g.55233514G= GRCh38
NC_000005.9:g.54529342G= , CM000667.1:g.54529342G= GRCh37
NC_000005.8:g.54565099G= NCBI36
NG_034201.1:g.5204C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.10C= MANE Select ENSP00000282572.4:p.Pro4=
ENST00000282572.4:c.10C= ENSP00000282572.4:p.Pro4=
ENST00000501463.2:c.10C= ENSP00000422485.1:p.Pro4=
NM_021147.4:c.10C= NP_066970.3:p.Pro4=
NR_125346.1:n.204C=
NR_125347.1:n.204C=
NM_021147.5:c.10C= MANE Select NP_066970.3:p.Pro4=
NR_125346.2:n.95C=
NR_125347.2:n.95C=