Canonical Allele Identifier: CA1547396769
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233273G= , CM000667.2:g.55233273G= GRCh38
NC_000005.9:g.54529101G= , CM000667.1:g.54529101G= GRCh37
NC_000005.8:g.54564858G= NCBI36
NG_034201.1:g.5445C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.251C= MANE Select ENSP00000282572.4:p.Pro84=
ENST00000282572.4:c.251C= ENSP00000282572.4:p.Pro84=
ENST00000501463.2:c.251C= ENSP00000422485.1:p.Pro84=
NM_021147.4:c.251C= NP_066970.3:p.Pro84=
NR_125346.1:n.445C=
NR_125347.1:n.445C=
NM_021147.5:c.251C= MANE Select NP_066970.3:p.Pro84=
NR_125346.2:n.336C=
NR_125347.2:n.336C=