Canonical Allele Identifier: CA2673856810
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233495-G-GA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233496dup , CM000667.2:g.55233496dup GRCh38
NC_000005.9:g.54529324dup , CM000667.1:g.54529324dup GRCh37
NC_000005.8:g.54565081dup NCBI36
NG_034201.1:g.5222dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.28dup MANE Select ENSP00000282572.4:p.Ser10PhefsTer?
ENST00000282572.4:c.28dup ENSP00000282572.4:p.Ser10PhefsTer?
ENST00000501463.2:c.28dup ENSP00000422485.1:p.Ser10PhefsTer?
NM_021147.4:c.28dup NP_066970.3:p.Ser10PhefsTer?
NR_125346.1:n.222dup
NR_125347.1:n.222dup
NM_021147.5:c.28dup MANE Select NP_066970.3:p.Ser10PhefsTer?
NR_125346.2:n.113dup
NR_125347.2:n.113dup
Search 100 bp 5'
Search 100 bp 3'