Canonical Allele Identifier: CA1547390685
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1745658716
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233363_55233373del , CM000667.2:g.55233363_55233373del GRCh38
NC_000005.9:g.54529191_54529201del , CM000667.1:g.54529191_54529201del GRCh37
NC_000005.8:g.54564948_54564958del NCBI36
NG_034201.1:g.5349_5359del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.155_165del MANE Select ENSP00000282572.4:p.Pro52ArgfsTer26
ENST00000282572.4:c.155_165del ENSP00000282572.4:p.Pro52ArgfsTer26
ENST00000501463.2:c.155_165del ENSP00000422485.1:p.Pro52ArgfsTer26
NM_021147.4:c.155_165del NP_066970.3:p.Pro52ArgfsTer26
NR_125346.1:n.349_359del
NR_125347.1:n.349_359del
NM_021147.5:c.155_165del MANE Select NP_066970.3:p.Pro52ArgfsTer26
NR_125346.2:n.240_250del
NR_125347.2:n.240_250del
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