Canonical Allele Identifier: CA2673856321

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232948-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232949_55232950del , CM000667.2:g.55232949_55232950del	GRCh38
NC_000005.9:g.54528777_54528778del , CM000667.1:g.54528777_54528778del	GRCh37
NC_000005.8:g.54564534_54564535del	NCBI36
NG_034201.1:g.5768_5769del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+193_381+194del MANE Select	ENSP00000282572.4:n.381+193_381+194del
ENST00000282572.4:c.381+193_381+194del	ENSP00000282572.4:n.381+193_381+194del
ENST00000501463.2:c.*178_*179del	ENSP00000422485.1:n.*178_*179del
NM_021147.4:c.381+193_381+194del	NP_066970.3:n.381+193_381+194del
NR_125346.1:n.768_769del
NR_125347.1:n.580+188_580+189del
NR_125348.1:n.42_43del
NM_021147.5:c.381+193_381+194del MANE Select	NP_066970.3:n.381+193_381+194del
NR_125346.2:n.659_660del
NR_125347.2:n.471+188_471+189del