Canonical Allele Identifier: CA1547396678
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233134G= , CM000667.2:g.55233134G= GRCh38
NC_000005.9:g.54528962G= , CM000667.1:g.54528962G= GRCh37
NC_000005.8:g.54564719G= NCBI36
NG_034201.1:g.5584C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+9C= MANE Select ENSP00000282572.4:n.381+9C=
ENST00000282572.4:c.381+9C= ENSP00000282572.4:n.381+9C=
ENST00000501463.2:c.390C= ENSP00000422485.1:p.Cys130=
NM_021147.4:c.381+9C= NP_066970.3:n.381+9C=
NR_125346.1:n.584C=
NR_125347.1:n.580+4C=
NM_021147.5:c.381+9C= MANE Select NP_066970.3:n.381+9C=
NR_125346.2:n.475C=
NR_125347.2:n.471+4C=