Canonical Allele Identifier: CA2564262971

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232920del , CM000667.2:g.55232920del	GRCh38
NC_000005.9:g.54528748del , CM000667.1:g.54528748del	GRCh37
NC_000005.8:g.54564505del	NCBI36
NG_034201.1:g.5799del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+224del MANE Select	ENSP00000282572.4:n.381+224del
ENST00000282572.4:c.381+224del	ENSP00000282572.4:n.381+224del
ENST00000501463.2:c.*209del	ENSP00000422485.1:n.*209del
NM_021147.4:c.381+224del	NP_066970.3:n.381+224del
NR_125346.1:n.799del
NR_125347.1:n.580+219del
NR_125348.1:n.73del
NM_021147.5:c.381+224del MANE Select	NP_066970.3:n.381+224del
NR_125346.2:n.690del
NR_125347.2:n.471+219del