Canonical Allele Identifier: CA1076233964

Gene: CCNO

Linked Data

• gnomAD v3: 5-55233575-C-CGCAGCCA
• gnomAD v4: 5-55233575-C-CGCAGCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55233575_55233576insGCAGCCA , CM000667.2:g.55233575_55233576insGCAGCCA	GRCh38
NC_000005.9:g.54529403_54529404insGCAGCCA , CM000667.1:g.54529403_54529404insGCAGCCA	GRCh37
NC_000005.8:g.54565160_54565161insGCAGCCA	NCBI36
NG_034201.1:g.5142_5143insTGGCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282572.5:c.-53_-52insTGGCTGC MANE Select	ENSP00000282572.4:n.-53_-52insTGGCTGC
ENST00000282572.4:c.-53_-52insTGGCTGC	ENSP00000282572.4:n.-53_-52insTGGCTGC
ENST00000501463.2:c.-53_-52insTGGCTGC	ENSP00000422485.1:n.-53_-52insTGGCTGC
NM_021147.4:c.-53_-52insTGGCTGC	NP_066970.3:n.-53_-52insTGGCTGC
NR_125346.1:n.142_143insTGGCTGC
NR_125347.1:n.142_143insTGGCTGC
NM_021147.5:c.-53_-52insTGGCTGC MANE Select	NP_066970.3:n.-53_-52insTGGCTGC
NR_125346.2:n.33_34insTGGCTGC
NR_125347.2:n.33_34insTGGCTGC