Canonical Allele Identifier: CA1547396585
Gene: CCNO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233002A= , CM000667.2:g.55233002A= GRCh38
NC_000005.9:g.54528830A= , CM000667.1:g.54528830A= GRCh37
NC_000005.8:g.54564587A= NCBI36
NG_034201.1:g.5716T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+141T= MANE Select ENSP00000282572.4:n.381+141T=
ENST00000282572.4:c.381+141T= ENSP00000282572.4:n.381+141T=
ENST00000501463.2:c.*126T= ENSP00000422485.1:n.*126T=
NM_021147.4:c.381+141T= NP_066970.3:n.381+141T=
NR_125346.1:n.716T=
NR_125347.1:n.580+136T=
NM_021147.5:c.381+141T= MANE Select NP_066970.3:n.381+141T=
NR_125346.2:n.607T=
NR_125347.2:n.471+136T=
Search 100 bp 5'
Search 100 bp 3'