Canonical Allele Identifier: CA2673856371

Gene: CCNO

Linked Data

• gnomAD v4: 5-55232991-G-GACC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232993_55232994insCAC , CM000667.2:g.55232993_55232994insCAC	GRCh38
NC_000005.9:g.54528821_54528822insCAC , CM000667.1:g.54528821_54528822insCAC	GRCh37
NC_000005.8:g.54564578_54564579insCAC	NCBI36
NG_034201.1:g.5726_5727insGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+151_381+152insGGT MANE Select	ENSP00000282572.4:n.381+151_381+152insGGT
ENST00000282572.4:c.381+151_381+152insGGT	ENSP00000282572.4:n.381+151_381+152insGGT
ENST00000501463.2:c.*136_*137insGGT	ENSP00000422485.1:n.*136_*137insGGT
NM_021147.4:c.381+151_381+152insGGT	NP_066970.3:n.381+151_381+152insGGT
NR_125346.1:n.726_727insGGT
NR_125347.1:n.580+146_580+147insGGT
NM_021147.5:c.381+151_381+152insGGT MANE Select	NP_066970.3:n.381+151_381+152insGGT
NR_125346.2:n.617_618insGGT
NR_125347.2:n.471+146_471+147insGGT