Canonical Allele Identifier: CA2673856802
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233280-GGCTACCACCCCGC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233283_55233295del , CM000667.2:g.55233283_55233295del GRCh38
NC_000005.9:g.54529111_54529123del , CM000667.1:g.54529111_54529123del GRCh37
NC_000005.8:g.54564868_54564880del NCBI36
NG_034201.1:g.5425_5437del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.231_243del MANE Select ENSP00000282572.4:p.Arg78ProfsTer12
ENST00000282572.4:c.231_243del ENSP00000282572.4:p.Arg78ProfsTer12
ENST00000501463.2:c.231_243del ENSP00000422485.1:p.Arg78ProfsTer12
NM_021147.4:c.231_243del NP_066970.3:p.Arg78ProfsTer12
NR_125346.1:n.425_437del
NR_125347.1:n.425_437del
NM_021147.5:c.231_243del MANE Select NP_066970.3:p.Arg78ProfsTer12
NR_125346.2:n.316_328del
NR_125347.2:n.316_328del
Search 100 bp 5'
Search 100 bp 3'