Canonical Allele Identifier: CA1547396781
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233287A= , CM000667.2:g.55233287A= GRCh38
NC_000005.9:g.54529115A= , CM000667.1:g.54529115A= GRCh37
NC_000005.8:g.54564872A= NCBI36
NG_034201.1:g.5431T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.237T= MANE Select ENSP00000282572.4:p.Gly79=
ENST00000282572.4:c.237T= ENSP00000282572.4:p.Gly79=
ENST00000501463.2:c.237T= ENSP00000422485.1:p.Gly79=
NM_021147.4:c.237T= NP_066970.3:p.Gly79=
NR_125346.1:n.431T=
NR_125347.1:n.431T=
NM_021147.5:c.237T= MANE Select NP_066970.3:p.Gly79=
NR_125346.2:n.322T=
NR_125347.2:n.322T=