Canonical Allele Identifier: CA2673856892

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233596-T-TGC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233598_55233599dup , CM000667.2:g.55233598_55233599dup	GRCh38
NC_000005.9:g.54529426_54529427dup , CM000667.1:g.54529426_54529427dup	GRCh37
NC_000005.8:g.54565183_54565184dup	NCBI36
NG_034201.1:g.5120_5121dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.-75_-74dup MANE Select	ENSP00000282572.4:n.-75_-74dup
ENST00000282572.4:c.-75_-74dup	ENSP00000282572.4:n.-75_-74dup
NM_021147.4:c.-75_-74dup	NP_066970.3:n.-75_-74dup
NR_125346.1:n.120_121dup
NR_125347.1:n.120_121dup
NM_021147.5:c.-75_-74dup MANE Select	NP_066970.3:n.-75_-74dup
NR_125346.2:n.11_12dup
NR_125347.2:n.11_12dup