Canonical Allele Identifier: CA1547396645

Gene: CCNO

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233092_55233093delinsTG , CM000667.2:g.55233092_55233093delinsTG	GRCh38
NC_000005.9:g.54528920_54528921delinsTG , CM000667.1:g.54528920_54528921delinsTG	GRCh37
NC_000005.8:g.54564677_54564678delinsTG	NCBI36
NG_034201.1:g.5625_5626delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+50_381+51delinsCA MANE Select	ENSP00000282572.4:n.381+50_381+51delinsCA
ENST00000282572.4:c.381+50_381+51delinsCA	ENSP00000282572.4:n.381+50_381+51delinsCA
ENST00000501463.2:c.*35_*36delinsCA	ENSP00000422485.1:n.*35_*36delinsCA
NM_021147.4:c.381+50_381+51delinsCA	NP_066970.3:n.381+50_381+51delinsCA
NR_125346.1:n.625_626delinsCA
NR_125347.1:n.580+45_580+46delinsCA
NM_021147.5:c.381+50_381+51delinsCA MANE Select	NP_066970.3:n.381+50_381+51delinsCA
NR_125346.2:n.516_517delinsCA
NR_125347.2:n.471+45_471+46delinsCA