Canonical Allele Identifier: CA345086
Gene: OTOF HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 65775
ClinVar RCV Id: RCV000056014
dbSNP Id: rs397515581

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26483623del , CM000664.2:g.26483623del GRCh38
NC_000002.11:g.26706491del , CM000664.1:g.26706491del GRCh37
NC_000002.10:g.26559995del NCBI36
NG_009937.1:g.80081del

Transcript Alleles

HGVS Amino-acid change
NM_001287489.1:c.1236del VV NP_001274418.1:p.Glu413AsnfsTer9
NM_194248.2:c.1236del VV NP_919224.1:p.Glu413AsnfsTer9
XM_005264644.2:n.1281del XP_005264701.1:p.Glu428AsnfsTer9
XM_011533185.1:n.1281del XP_011531487.1:p.Glu428AsnfsTer9
XM_017005338.1:n.1236del XP_016860827.1:p.Glu413AsnfsTer9
ENST00000272371.6:c.1236del ENSP00000272371.2:p.Glu413AsnfsTer9
ENST00000403946.7:c.1236del ENSP00000385255.3:p.Glu413AsnfsTer9