Canonical Allele Identifier: CA2673856412

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233022-T-TCGGGGCGGGACCTGGGCTGTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233027_55233048dup , CM000667.2:g.55233027_55233048dup	GRCh38
NC_000005.9:g.54528855_54528876dup , CM000667.1:g.54528855_54528876dup	GRCh37
NC_000005.8:g.54564612_54564633dup	NCBI36
NG_034201.1:g.5674_5695dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+99_381+120dup MANE Select	ENSP00000282572.4:n.381+99_381+120dup
ENST00000282572.4:c.381+99_381+120dup	ENSP00000282572.4:n.381+99_381+120dup
ENST00000501463.2:c.*84_*105dup	ENSP00000422485.1:n.*84_*105dup
NM_021147.4:c.381+99_381+120dup	NP_066970.3:n.381+99_381+120dup
NR_125346.1:n.674_695dup
NR_125347.1:n.580+94_580+115dup
NM_021147.5:c.381+99_381+120dup MANE Select	NP_066970.3:n.381+99_381+120dup
NR_125346.2:n.565_586dup
NR_125347.2:n.471+94_471+115dup