Canonical Allele Identifier: CA1547390974
Gene: CCNO HGNC NCBI

Linked Data

dbSNP Id: rs1745671555

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233588del , CM000667.2:g.55233588del GRCh38
NC_000005.9:g.54529416del , CM000667.1:g.54529416del GRCh37
NC_000005.8:g.54565173del NCBI36
NG_034201.1:g.5130del

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.-65del MANE Select ENSP00000282572.4:n.-65del
ENST00000282572.4:c.-65del ENSP00000282572.4:n.-65del
ENST00000501463.2:c.-65del ENSP00000422485.1:n.-65del
NM_021147.4:c.-65del NP_066970.3:n.-65del
NR_125346.1:n.130del
NR_125347.1:n.130del
NM_021147.5:c.-65del MANE Select NP_066970.3:n.-65del
NR_125346.2:n.21del
NR_125347.2:n.21del