Canonical Allele Identifier: CA2549422592
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233620_55233621insGG , CM000667.2:g.55233620_55233621insGG GRCh38
NC_000005.9:g.54529448_54529449insGG , CM000667.1:g.54529448_54529449insGG GRCh37
NC_000005.8:g.54565205_54565206insGG NCBI36
NG_034201.1:g.5097_5098insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.4:c.-98_-97insCC ENSP00000282572.4:n.-98_-97insCC
NM_021147.4:c.-98_-97insCC NP_066970.3:n.-98_-97insCC
NR_125346.1:n.97_98insCC
NR_125347.1:n.97_98insCC
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