Canonical Allele Identifier: CA2673856306
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232933_55232934dup , CM000667.2:g.55232933_55232934dup GRCh38
NC_000005.9:g.54528761_54528762dup , CM000667.1:g.54528761_54528762dup GRCh37
NC_000005.8:g.54564518_54564519dup NCBI36
NG_034201.1:g.5786_5787dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+211_381+212dup MANE Select ENSP00000282572.4:n.381+211_381+212dup
ENST00000282572.4:c.381+211_381+212dup ENSP00000282572.4:n.381+211_381+212dup
ENST00000501463.2:c.*196_*197dup ENSP00000422485.1:n.*196_*197dup
NM_021147.4:c.381+211_381+212dup NP_066970.3:n.381+211_381+212dup
NR_125346.1:n.786_787dup
NR_125347.1:n.580+206_580+207dup
NR_125348.1:n.60_61dup
NM_021147.5:c.381+211_381+212dup MANE Select NP_066970.3:n.381+211_381+212dup
NR_125346.2:n.677_678dup
NR_125347.2:n.471+206_471+207dup