Canonical Allele Identifier: CA2673856290
Gene: CCNO HGNC NCBI

Linked Data

gnomAD v4: 5-55232914-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55232914A>T , CM000667.2:g.55232914A>T GRCh38
NC_000005.9:g.54528742A>T , CM000667.1:g.54528742A>T GRCh37
NC_000005.8:g.54564499A>T NCBI36
NG_034201.1:g.5804T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.381+229T>A MANE Select ENSP00000282572.4:n.381+229T>A
ENST00000282572.4:c.381+229T>A ENSP00000282572.4:n.381+229T>A
ENST00000501463.2:c.*214T>A ENSP00000422485.1:n.*214T>A
NM_021147.4:c.381+229T>A NP_066970.3:n.381+229T>A
NR_125346.1:n.804T>A
NR_125347.1:n.580+224T>A
NR_125348.1:n.78T>A
NM_021147.5:c.381+229T>A MANE Select NP_066970.3:n.381+229T>A
NR_125346.2:n.695T>A
NR_125347.2:n.471+224T>A