Canonical Allele Identifier: CA559800482
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1197002221
gnomAD v2: 5-54529257-CTCT-C
gnomAD v3: 5-55233429-CTCT-C
gnomAD v4: 5-55233429-CTCT-C
MyVariant Identifiers: chr5:g.54529258_54529260del (hg19) chr5:g.55233430_55233432del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233435_55233437del , CM000667.2:g.55233435_55233437del GRCh38
NC_000005.9:g.54529263_54529265del , CM000667.1:g.54529263_54529265del GRCh37
NC_000005.8:g.54565020_54565022del NCBI36
NG_034201.1:g.5286_5288del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.92_94del MANE Select ENSP00000282572.4:p.Lys31del
ENST00000282572.4:c.92_94del ENSP00000282572.4:p.Lys31del
ENST00000501463.2:c.92_94del ENSP00000422485.1:p.Lys31del
NM_021147.4:c.92_94del NP_066970.3:p.Lys31del
NR_125346.1:n.286_288del
NR_125347.1:n.286_288del
NM_021147.5:c.92_94del MANE Select NP_066970.3:p.Lys31del
NR_125346.2:n.177_179del
NR_125347.2:n.177_179del
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