Canonical Allele Identifier: CA3266830
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs778453227
ExAC: 5:54529111 TACC / T
gnomAD v2: 5-54529111-TACC-T
gnomAD v3: 5-55233283-TACC-T
gnomAD v4: 5-55233283-TACC-T
MyVariant Identifiers: chr5:g.54529112_54529114del (hg19) chr5:g.55233284_55233286del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233287_55233289del , CM000667.2:g.55233287_55233289del GRCh38
NC_000005.9:g.54529115_54529117del , CM000667.1:g.54529115_54529117del GRCh37
NC_000005.8:g.54564872_54564874del NCBI36
NG_034201.1:g.5432_5434del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.238_240del MANE Select ENSP00000282572.4:p.Gly80del
ENST00000282572.4:c.238_240del ENSP00000282572.4:p.Gly80del
ENST00000501463.2:c.238_240del ENSP00000422485.1:p.Gly80del
NM_021147.4:c.238_240del NP_066970.3:p.Gly80del
NR_125346.1:n.432_434del
NR_125347.1:n.432_434del
NM_021147.5:c.238_240del MANE Select NP_066970.3:p.Gly80del
NR_125346.2:n.323_325del
NR_125347.2:n.323_325del
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