Canonical Allele Identifier: CA2578309964
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233525-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233526dup , CM000667.2:g.55233526dup GRCh38
NC_000005.9:g.54529354dup , CM000667.1:g.54529354dup GRCh37
NC_000005.8:g.54565111dup NCBI36
NG_034201.1:g.5192dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-3dup MANE Select ENSP00000282572.4:n.-3dup
ENST00000282572.4:c.-3dup ENSP00000282572.4:n.-3dup
ENST00000501463.2:c.-3dup ENSP00000422485.1:n.-3dup
NM_021147.4:c.-3dup NP_066970.3:n.-3dup
NR_125346.1:n.192dup
NR_125347.1:n.192dup
NM_021147.5:c.-3dup MANE Select NP_066970.3:n.-3dup
NR_125346.2:n.83dup
NR_125347.2:n.83dup
Search 100 bp 5'
Search 100 bp 3'