Canonical Allele Identifier: CA2673856485
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233082-GGA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233088_55233089del , CM000667.2:g.55233088_55233089del GRCh38
NC_000005.9:g.54528916_54528917del , CM000667.1:g.54528916_54528917del GRCh37
NC_000005.8:g.54564673_54564674del NCBI36
NG_034201.1:g.5634_5635del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+59_381+60del MANE Select ENSP00000282572.4:n.381+59_381+60del
ENST00000282572.4:c.381+59_381+60del ENSP00000282572.4:n.381+59_381+60del
ENST00000501463.2:c.*44_*45del ENSP00000422485.1:n.*44_*45del
NM_021147.4:c.381+59_381+60del NP_066970.3:n.381+59_381+60del
NR_125346.1:n.634_635del
NR_125347.1:n.580+54_580+55del
NM_021147.5:c.381+59_381+60del MANE Select NP_066970.3:n.381+59_381+60del
NR_125346.2:n.525_526del
NR_125347.2:n.471+54_471+55del
Search 100 bp 5'
Search 100 bp 3'