Canonical Allele Identifier: CA359725858
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55233434-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55233434C>A , CM000667.2:g.55233434C>A GRCh38
NC_000005.9:g.54529262C>A , CM000667.1:g.54529262C>A GRCh37
NC_000005.8:g.54565019C>A NCBI36
NG_034201.1:g.5284G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.90G>T MANE Select ENSP00000282572.4:p.Lys30Asn
ENST00000282572.4:c.90G>T ENSP00000282572.4:p.Lys30Asn
ENST00000501463.2:c.90G>T ENSP00000422485.1:p.Lys30Asn
NM_021147.4:c.90G>T NP_066970.3:p.Lys30Asn
NR_125346.1:n.284G>T
NR_125347.1:n.284G>T
NM_021147.5:c.90G>T MANE Select NP_066970.3:p.Lys30Asn
NR_125346.2:n.175G>T
NR_125347.2:n.175G>T