Canonical Allele Identifier: CA1239831425
Gene: OTOF HGNC NCBI

Linked Data

dbSNP Id: rs1665655962

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26484591del , CM000664.2:g.26484591del GRCh38
NC_000002.11:g.26707459del , CM000664.1:g.26707459del GRCh37
NC_000002.10:g.26560963del NCBI36
NG_009937.1:g.79108del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1088del MANE Select ENSP00000272371.2:p.Asp363ValfsTer7
ENST00000272371.6:c.1088del ENSP00000272371.2:p.Asp363ValfsTer7
ENST00000403946.7:c.1088del ENSP00000385255.3:p.Asp363ValfsTer7
NM_001287489.1:c.1088del NP_001274418.1:p.Asp363ValfsTer7
NM_194248.2:c.1088del NP_919224.1:p.Asp363ValfsTer7
XM_005264644.2:c.1133del XP_005264701.1:p.Asp378ValfsTer7
XM_011533185.1:c.1133del XP_011531487.1:p.Asp378ValfsTer7
XM_017005338.1:c.1088del XP_016860827.1:p.Asp363ValfsTer7
NM_001287489.2:c.1088del NP_001274418.1:p.Asp363ValfsTer7
NM_194248.3:c.1088del MANE Select NP_919224.1:p.Asp363ValfsTer7