Canonical Allele Identifier: CA1547390979

Gene: CCNO

Linked Data

• dbSNP Id: rs1745671895
• gnomAD v4: 5-55233589-TCGAAAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233590_55233595del , CM000667.2:g.55233590_55233595del	GRCh38
NC_000005.9:g.54529418_54529423del , CM000667.1:g.54529418_54529423del	GRCh37
NC_000005.8:g.54565175_54565180del	NCBI36
NG_034201.1:g.5123_5128del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.-72_-67del MANE Select	ENSP00000282572.4:n.-72_-67del
ENST00000282572.4:c.-72_-67del	ENSP00000282572.4:n.-72_-67del
ENST00000501463.2:c.-72_-67del	ENSP00000422485.1:n.-72_-67del
NM_021147.4:c.-72_-67del	NP_066970.3:n.-72_-67del
NR_125346.1:n.123_128del
NR_125347.1:n.123_128del
NM_021147.5:c.-72_-67del MANE Select	NP_066970.3:n.-72_-67del
NR_125346.2:n.14_19del
NR_125347.2:n.14_19del