Canonical Allele Identifier: CA2578309962
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233439_55233442dup , CM000667.2:g.55233439_55233442dup GRCh38
NC_000005.9:g.54529267_54529270dup , CM000667.1:g.54529267_54529270dup GRCh37
NC_000005.8:g.54565024_54565027dup NCBI36
NG_034201.1:g.5276_5279dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.82_85dup MANE Select ENSP00000282572.4:p.Val29AlafsTer?
ENST00000282572.4:c.82_85dup ENSP00000282572.4:p.Val29AlafsTer?
ENST00000501463.2:c.82_85dup ENSP00000422485.1:p.Val29AlafsTer?
NM_021147.4:c.82_85dup NP_066970.3:p.Val29AlafsTer?
NR_125346.1:n.276_279dup
NR_125347.1:n.276_279dup
NM_021147.5:c.82_85dup MANE Select NP_066970.3:p.Val29AlafsTer?
NR_125346.2:n.167_170dup
NR_125347.2:n.167_170dup
Search 100 bp 5'
Search 100 bp 3'