Canonical Allele Identifier: CA1547390914
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233532C= , CM000667.2:g.55233532C= GRCh38
NC_000005.9:g.54529360C= , CM000667.1:g.54529360C= GRCh37
NC_000005.8:g.54565117C= NCBI36
NG_034201.1:g.5186G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-9G= MANE Select ENSP00000282572.4:n.-9G=
ENST00000282572.4:c.-9G= ENSP00000282572.4:n.-9G=
ENST00000501463.2:c.-9G= ENSP00000422485.1:n.-9G=
NM_021147.4:c.-9G= NP_066970.3:n.-9G=
NR_125346.1:n.186G=
NR_125347.1:n.186G=
NM_021147.5:c.-9G= MANE Select NP_066970.3:n.-9G=
NR_125346.2:n.77G=
NR_125347.2:n.77G=