Canonical Allele Identifier: CA3266840
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs752106293
ExAC: 5:54529159 T / TG
gnomAD v2: 5-54529159-T-TG
gnomAD v3: 5-55233331-T-TG
gnomAD v4: 5-55233331-T-TG
MyVariant Identifiers: chr5:g.54529159_54529160insG (hg19) chr5:g.55233331_55233332insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233336dup , CM000667.2:g.55233336dup GRCh38
NC_000005.9:g.54529164dup , CM000667.1:g.54529164dup GRCh37
NC_000005.8:g.54564921dup NCBI36
NG_034201.1:g.5386dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.192dup MANE Select ENSP00000282572.4:p.Ser65GlnfsTer17
ENST00000282572.4:c.192dup ENSP00000282572.4:p.Ser65GlnfsTer17
ENST00000501463.2:c.192dup ENSP00000422485.1:p.Ser65GlnfsTer17
NM_021147.4:c.192dup NP_066970.3:p.Ser65GlnfsTer17
NR_125346.1:n.386dup
NR_125347.1:n.386dup
NM_021147.5:c.192dup MANE Select NP_066970.3:p.Ser65GlnfsTer17
NR_125346.2:n.277dup
NR_125347.2:n.277dup
Search 100 bp 5'
Search 100 bp 3'