Canonical Allele Identifier: CA1547396618

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233059_55233079delinsCGGAGGGCCGAGCCGGCAGGA , CM000667.2:g.55233059_55233079delinsCGGAGGGCCGAGCCGGCAGGA	GRCh38
NC_000005.9:g.54528887_54528907delinsCGGAGGGCCGAGCCGGCAGGA , CM000667.1:g.54528887_54528907delinsCGGAGGGCCGAGCCGGCAGGA	GRCh37
NC_000005.8:g.54564644_54564664delinsCGGAGGGCCGAGCCGGCAGGA	NCBI36
NG_034201.1:g.5639_5659delinsTCCTGCCGGCTCGGCCCTCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+64_381+84delinsTCCTGCCGGCTCGGCCCTCCG MANE Select	ENSP00000282572.4:n.381+64_381+84delinsTCCTGCCGGCTCGGCCCTCCG
ENST00000282572.4:c.381+64_381+84delinsTCCTGCCGGCTCGGCCCTCCG	ENSP00000282572.4:n.381+64_381+84delinsTCCTGCCGGCTCGGCCCTCCG
ENST00000501463.2:c.*49_*69delinsTCCTGCCGGCTCGGCCCTCCG	ENSP00000422485.1:n.*49_*69delinsTCCTGCCGGCTCGGCCCTCCG
NM_021147.4:c.381+64_381+84delinsTCCTGCCGGCTCGGCCCTCCG	NP_066970.3:n.381+64_381+84delinsTCCTGCCGGCTCGGCCCTCCG
NR_125346.1:n.639_659delinsTCCTGCCGGCTCGGCCCTCCG
NR_125347.1:n.580+59_580+79delinsTCCTGCCGGCTCGGCCCTCCG
NM_021147.5:c.381+64_381+84delinsTCCTGCCGGCTCGGCCCTCCG MANE Select	NP_066970.3:n.381+64_381+84delinsTCCTGCCGGCTCGGCCCTCCG
NR_125346.2:n.530_550delinsTCCTGCCGGCTCGGCCCTCCG
NR_125347.2:n.471+59_471+79delinsTCCTGCCGGCTCGGCCCTCCG