Canonical Allele Identifier: CA2673856304
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232929-ACGG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232930_55232932del , CM000667.2:g.55232930_55232932del GRCh38
NC_000005.9:g.54528758_54528760del , CM000667.1:g.54528758_54528760del GRCh37
NC_000005.8:g.54564515_54564517del NCBI36
NG_034201.1:g.5786_5788del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+211_381+213del MANE Select ENSP00000282572.4:n.381+211_381+213del
ENST00000282572.4:c.381+211_381+213del ENSP00000282572.4:n.381+211_381+213del
ENST00000501463.2:c.*196_*198del ENSP00000422485.1:n.*196_*198del
NM_021147.4:c.381+211_381+213del NP_066970.3:n.381+211_381+213del
NR_125346.1:n.786_788del
NR_125347.1:n.580+206_580+208del
NR_125348.1:n.60_62del
NM_021147.5:c.381+211_381+213del MANE Select NP_066970.3:n.381+211_381+213del
NR_125346.2:n.677_679del
NR_125347.2:n.471+206_471+208del
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