Canonical Allele Identifier: CA1547396546
Gene: CCNO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232930C= , CM000667.2:g.55232930C= GRCh38
NC_000005.9:g.54528758C= , CM000667.1:g.54528758C= GRCh37
NC_000005.8:g.54564515C= NCBI36
NG_034201.1:g.5788G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+213G= MANE Select ENSP00000282572.4:n.381+213G=
ENST00000282572.4:c.381+213G= ENSP00000282572.4:n.381+213G=
ENST00000501463.2:c.*198G= ENSP00000422485.1:n.*198G=
NM_021147.4:c.381+213G= NP_066970.3:n.381+213G=
NR_125346.1:n.788G=
NR_125347.1:n.580+208G=
NR_125348.1:n.62G=
NM_021147.5:c.381+213G= MANE Select NP_066970.3:n.381+213G=
NR_125346.2:n.679G=
NR_125347.2:n.471+208G=