Canonical Allele Identifier: CA1547390814
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233460_55233463delinsCGTT , CM000667.2:g.55233460_55233463delinsCGTT GRCh38
NC_000005.9:g.54529288_54529291delinsCGTT , CM000667.1:g.54529288_54529291delinsCGTT GRCh37
NC_000005.8:g.54565045_54565048delinsCGTT NCBI36
NG_034201.1:g.5255_5258delinsAACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.61_64delinsAACG MANE Select ENSP00000282572.4:p.Asn21=
ENST00000282572.4:c.61_64delinsAACG ENSP00000282572.4:p.Asn21=
ENST00000501463.2:c.61_64delinsAACG ENSP00000422485.1:p.Asn21=
NM_021147.4:c.61_64delinsAACG NP_066970.3:p.Asn21=
NR_125346.1:n.255_258delinsAACG
NR_125347.1:n.255_258delinsAACG
NM_021147.5:c.61_64delinsAACG MANE Select NP_066970.3:p.Asn21=
NR_125346.2:n.146_149delinsAACG
NR_125347.2:n.146_149delinsAACG
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