Canonical Allele Identifier: CA1076233602

Gene: CCNO

Linked Data

• dbSNP Id: rs1745636086
• gnomAD v3: 5-55232920-C-CAGT
• gnomAD v4: 5-55232920-C-CAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55232922_55232923insTAG , CM000667.2:g.55232922_55232923insTAG	GRCh38
NC_000005.9:g.54528750_54528751insTAG , CM000667.1:g.54528750_54528751insTAG	GRCh37
NC_000005.8:g.54564507_54564508insTAG	NCBI36
NG_034201.1:g.5797_5798insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+222_381+223insACT MANE Select	ENSP00000282572.4:n.381+222_381+223insACT
ENST00000282572.4:c.381+222_381+223insACT	ENSP00000282572.4:n.381+222_381+223insACT
ENST00000501463.2:c.*207_*208insACT	ENSP00000422485.1:n.*207_*208insACT
NM_021147.4:c.381+222_381+223insACT	NP_066970.3:n.381+222_381+223insACT
NR_125346.1:n.797_798insACT
NR_125347.1:n.580+217_580+218insACT
NR_125348.1:n.71_72insACT
NM_021147.5:c.381+222_381+223insACT MANE Select	NP_066970.3:n.381+222_381+223insACT
NR_125346.2:n.688_689insACT
NR_125347.2:n.471+217_471+218insACT