Canonical Allele Identifier: CA2673856985

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233664-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233669dup , CM000667.2:g.55233669dup	GRCh38
NC_000005.9:g.54529497dup , CM000667.1:g.54529497dup	GRCh37
NC_000005.8:g.54565254dup	NCBI36
NG_034201.1:g.5053dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.4:c.-142dup	ENSP00000282572.4:n.-142dup
NM_021147.4:c.-142dup	NP_066970.3:n.-142dup
NR_125346.1:n.53dup
NR_125347.1:n.53dup