Canonical Allele Identifier: CA812218159

Gene: CCNO

Linked Data

• dbSNP Id: rs1250449574
• gnomAD v3: 5-55233059-CGGAGGGCCGAGCCGGCAGGA-C
• gnomAD v4: 5-55233059-CGGAGGGCCGAGCCGGCAGGA-C
• MyVariant Identifiers: chr5:g.54528888_54528907del (hg19) ; chr5:g.55233060_55233079del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233061_55233080del , CM000667.2:g.55233061_55233080del	GRCh38
NC_000005.9:g.54528889_54528908del , CM000667.1:g.54528889_54528908del	GRCh37
NC_000005.8:g.54564646_54564665del	NCBI36
NG_034201.1:g.5639_5658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.381+64_381+83del MANE Select	ENSP00000282572.4:n.381+64_381+83del
ENST00000282572.4:c.381+64_381+83del	ENSP00000282572.4:n.381+64_381+83del
ENST00000501463.2:c.*49_*68del	ENSP00000422485.1:n.*49_*68del
NM_021147.4:c.381+64_381+83del	NP_066970.3:n.381+64_381+83del
NR_125346.1:n.639_658del
NR_125347.1:n.580+59_580+78del
NM_021147.5:c.381+64_381+83del MANE Select	NP_066970.3:n.381+64_381+83del
NR_125346.2:n.530_549del
NR_125347.2:n.471+59_471+78del