Canonical Allele Identifier: CA1547390778
Gene: CCNO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233429_55233432delinsCTCT , CM000667.2:g.55233429_55233432delinsCTCT GRCh38
NC_000005.9:g.54529257_54529260delinsCTCT , CM000667.1:g.54529257_54529260delinsCTCT GRCh37
NC_000005.8:g.54565014_54565017delinsCTCT NCBI36
NG_034201.1:g.5286_5289delinsAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.92_95delinsAGAG MANE Select ENSP00000282572.4:p.Lys31=
ENST00000282572.4:c.92_95delinsAGAG ENSP00000282572.4:p.Lys31=
ENST00000501463.2:c.92_95delinsAGAG ENSP00000422485.1:p.Lys31=
NM_021147.4:c.92_95delinsAGAG NP_066970.3:p.Lys31=
NR_125346.1:n.286_289delinsAGAG
NR_125347.1:n.286_289delinsAGAG
NM_021147.5:c.92_95delinsAGAG MANE Select NP_066970.3:p.Lys31=
NR_125346.2:n.177_180delinsAGAG
NR_125347.2:n.177_180delinsAGAG
Search 100 bp 5'
Search 100 bp 3'