Canonical Allele Identifier: CA2673856422

Gene: CCNO

Linked Data

• gnomAD v4: 5-55233030-G-GGACCTGGGCTGTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233043_55233044insCGACCTGGGCTGTC , CM000667.2:g.55233043_55233044insCGACCTGGGCTGTC	GRCh38
NC_000005.9:g.54528871_54528872insCGACCTGGGCTGTC , CM000667.1:g.54528871_54528872insCGACCTGGGCTGTC	GRCh37
NC_000005.8:g.54564628_54564629insCGACCTGGGCTGTC	NCBI36
NG_034201.1:g.5687_5688insGGACAGCCCAGGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+112_381+113insGGACAGCCCAGGTC MANE Select	ENSP00000282572.4:n.381+112_381+113insGGACAGCCCAGGTC
ENST00000282572.4:c.381+112_381+113insGGACAGCCCAGGTC	ENSP00000282572.4:n.381+112_381+113insGGACAGCCCAGGTC
ENST00000501463.2:c.*97_*98insGGACAGCCCAGGTC	ENSP00000422485.1:n.*97_*98insGGACAGCCCAGGTC
NM_021147.4:c.381+112_381+113insGGACAGCCCAGGTC	NP_066970.3:n.381+112_381+113insGGACAGCCCAGGTC
NR_125346.1:n.687_688insGGACAGCCCAGGTC
NR_125347.1:n.580+107_580+108insGGACAGCCCAGGTC
NM_021147.5:c.381+112_381+113insGGACAGCCCAGGTC MANE Select	NP_066970.3:n.381+112_381+113insGGACAGCCCAGGTC
NR_125346.2:n.578_579insGGACAGCCCAGGTC
NR_125347.2:n.471+107_471+108insGGACAGCCCAGGTC