Canonical Allele Identifier: CA118944768
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs376973189
gnomAD v2: 5-54528889-G-GC
gnomAD v3: 5-55233061-G-GC
gnomAD v4: 5-55233061-G-GC
MyVariant Identifiers: chr5:g.54528889_54528890insC (hg19) chr5:g.55233061_55233062insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233061_55233062insC , CM000667.2:g.55233061_55233062insC GRCh38
NC_000005.9:g.54528889_54528890insC , CM000667.1:g.54528889_54528890insC GRCh37
NC_000005.8:g.54564646_54564647insC NCBI36
NG_034201.1:g.5656_5657insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+81_381+82insG MANE Select ENSP00000282572.4:n.381+81_381+82insG
ENST00000282572.4:c.381+81_381+82insG ENSP00000282572.4:n.381+81_381+82insG
ENST00000501463.2:c.*66_*67insG ENSP00000422485.1:n.*66_*67insG
NM_021147.4:c.381+81_381+82insG NP_066970.3:n.381+81_381+82insG
NR_125346.1:n.656_657insG
NR_125347.1:n.580+76_580+77insG
NM_021147.5:c.381+81_381+82insG MANE Select NP_066970.3:n.381+81_381+82insG
NR_125346.2:n.547_548insG
NR_125347.2:n.471+76_471+77insG
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