Canonical Allele Identifier: CA1547390957
Gene: CCNO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233578C= , CM000667.2:g.55233578C= GRCh38
NC_000005.9:g.54529406C= , CM000667.1:g.54529406C= GRCh37
NC_000005.8:g.54565163C= NCBI36
NG_034201.1:g.5140G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-55G= MANE Select ENSP00000282572.4:n.-55G=
ENST00000282572.4:c.-55G= ENSP00000282572.4:n.-55G=
ENST00000501463.2:c.-55G= ENSP00000422485.1:n.-55G=
NM_021147.4:c.-55G= NP_066970.3:n.-55G=
NR_125346.1:n.140G=
NR_125347.1:n.140G=
NM_021147.5:c.-55G= MANE Select NP_066970.3:n.-55G=
NR_125346.2:n.31G=
NR_125347.2:n.31G=
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