Canonical Allele Identifier: CA359726001
Gene: CCNO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233453T>A , CM000667.2:g.55233453T>A GRCh38
NC_000005.9:g.54529281T>A , CM000667.1:g.54529281T>A GRCh37
NC_000005.8:g.54565038T>A NCBI36
NG_034201.1:g.5265A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.71A>T MANE Select ENSP00000282572.4:p.Asn24Ile
ENST00000282572.4:c.71A>T ENSP00000282572.4:p.Asn24Ile
ENST00000501463.2:c.71A>T ENSP00000422485.1:p.Asn24Ile
NM_021147.4:c.71A>T NP_066970.3:p.Asn24Ile
NR_125346.1:n.265A>T
NR_125347.1:n.265A>T
NM_021147.5:c.71A>T MANE Select NP_066970.3:p.Asn24Ile
NR_125346.2:n.156A>T
NR_125347.2:n.156A>T