Canonical Allele Identifier: CA444397319
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233391-GA-G
MyVariant Identifiers: chr5:g.54529220del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233392del , CM000667.2:g.55233392del GRCh38
NC_000005.9:g.54529220del , CM000667.1:g.54529220del GRCh37
NC_000005.8:g.54564977del NCBI36
NG_034201.1:g.5326del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.132del MANE Select ENSP00000282572.4:p.Leu46Ter
ENST00000282572.4:c.132del ENSP00000282572.4:p.Leu46Ter
ENST00000501463.2:c.132del ENSP00000422485.1:p.Leu46Ter
NM_021147.4:c.132del NP_066970.3:p.Leu46Ter
NR_125346.1:n.326del
NR_125347.1:n.326del
NM_021147.5:c.132del MANE Select NP_066970.3:p.Leu46Ter
NR_125346.2:n.217del
NR_125347.2:n.217del
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