Canonical Allele Identifier: CA1547390885
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233508G= , CM000667.2:g.55233508G= GRCh38
NC_000005.9:g.54529336G= , CM000667.1:g.54529336G= GRCh37
NC_000005.8:g.54565093G= NCBI36
NG_034201.1:g.5210C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.16C= MANE Select ENSP00000282572.4:p.Pro6=
ENST00000282572.4:c.16C= ENSP00000282572.4:p.Pro6=
ENST00000501463.2:c.16C= ENSP00000422485.1:p.Pro6=
NM_021147.4:c.16C= NP_066970.3:p.Pro6=
NR_125346.1:n.210C=
NR_125347.1:n.210C=
NM_021147.5:c.16C= MANE Select NP_066970.3:p.Pro6=
NR_125346.2:n.101C=
NR_125347.2:n.101C=