Canonical Allele Identifier: CA1547396547
Gene: CCNO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232931G= , CM000667.2:g.55232931G= GRCh38
NC_000005.9:g.54528759G= , CM000667.1:g.54528759G= GRCh37
NC_000005.8:g.54564516G= NCBI36
NG_034201.1:g.5787C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+212C= MANE Select ENSP00000282572.4:n.381+212C=
ENST00000282572.4:c.381+212C= ENSP00000282572.4:n.381+212C=
ENST00000501463.2:c.*197C= ENSP00000422485.1:n.*197C=
NM_021147.4:c.381+212C= NP_066970.3:n.381+212C=
NR_125346.1:n.787C=
NR_125347.1:n.580+207C=
NR_125348.1:n.61C=
NM_021147.5:c.381+212C= MANE Select NP_066970.3:n.381+212C=
NR_125346.2:n.678C=
NR_125347.2:n.471+207C=
Search 100 bp 5'
Search 100 bp 3'