Canonical Allele Identifier: CA2673856354

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232981-TGAGGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232983_55232988del , CM000667.2:g.55232983_55232988del	GRCh38
NC_000005.9:g.54528811_54528816del , CM000667.1:g.54528811_54528816del	GRCh37
NC_000005.8:g.54564568_54564573del	NCBI36
NG_034201.1:g.5731_5736del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+156_381+161del MANE Select	ENSP00000282572.4:n.381+156_381+161del
ENST00000282572.4:c.381+156_381+161del	ENSP00000282572.4:n.381+156_381+161del
ENST00000501463.2:c.*141_*146del	ENSP00000422485.1:n.*141_*146del
NM_021147.4:c.381+156_381+161del	NP_066970.3:n.381+156_381+161del
NR_125346.1:n.731_736del
NR_125347.1:n.580+151_580+156del
NR_125348.1:n.5_10del
NM_021147.5:c.381+156_381+161del MANE Select	NP_066970.3:n.381+156_381+161del
NR_125346.2:n.622_627del
NR_125347.2:n.471+151_471+156del