Canonical Allele Identifier: CA2673856331

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232956-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232960del , CM000667.2:g.55232960del	GRCh38
NC_000005.9:g.54528788del , CM000667.1:g.54528788del	GRCh37
NC_000005.8:g.54564545del	NCBI36
NG_034201.1:g.5761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+186del MANE Select	ENSP00000282572.4:n.381+186del
ENST00000282572.4:c.381+186del	ENSP00000282572.4:n.381+186del
ENST00000501463.2:c.*171del	ENSP00000422485.1:n.*171del
NM_021147.4:c.381+186del	NP_066970.3:n.381+186del
NR_125346.1:n.761del
NR_125347.1:n.580+181del
NR_125348.1:n.35del
NM_021147.5:c.381+186del MANE Select	NP_066970.3:n.381+186del
NR_125346.2:n.652del
NR_125347.2:n.471+181del