Canonical Allele Identifier: CA1547396753
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233259G= , CM000667.2:g.55233259G= GRCh38
NC_000005.9:g.54529087G= , CM000667.1:g.54529087G= GRCh37
NC_000005.8:g.54564844G= NCBI36
NG_034201.1:g.5459C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.265C= MANE Select ENSP00000282572.4:p.Pro89=
ENST00000282572.4:c.265C= ENSP00000282572.4:p.Pro89=
ENST00000501463.2:c.265C= ENSP00000422485.1:p.Pro89=
NM_021147.4:c.265C= NP_066970.3:p.Pro89=
NR_125346.1:n.459C=
NR_125347.1:n.459C=
NM_021147.5:c.265C= MANE Select NP_066970.3:p.Pro89=
NR_125346.2:n.350C=
NR_125347.2:n.350C=