Canonical Allele Identifier: CA2673856377

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232994-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232998del , CM000667.2:g.55232998del	GRCh38
NC_000005.9:g.54528826del , CM000667.1:g.54528826del	GRCh37
NC_000005.8:g.54564583del	NCBI36
NG_034201.1:g.5723del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+148del MANE Select	ENSP00000282572.4:n.381+148del
ENST00000282572.4:c.381+148del	ENSP00000282572.4:n.381+148del
ENST00000501463.2:c.*133del	ENSP00000422485.1:n.*133del
NM_021147.4:c.381+148del	NP_066970.3:n.381+148del
NR_125346.1:n.723del
NR_125347.1:n.580+143del
NM_021147.5:c.381+148del MANE Select	NP_066970.3:n.381+148del
NR_125346.2:n.614del
NR_125347.2:n.471+143del