Canonical Allele Identifier: CA2658240195
Gene: OTOF HGNC NCBI

Linked Data

gnomAD v4: 2-26484762-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26484763del , CM000664.2:g.26484763del GRCh38
NC_000002.11:g.26707631del , CM000664.1:g.26707631del GRCh37
NC_000002.10:g.26561135del NCBI36
NG_009937.1:g.78936del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1046-130del MANE Select ENSP00000272371.2:n.1046-130del
ENST00000272371.6:c.1046-130del ENSP00000272371.2:n.1046-130del
ENST00000403946.7:c.1046-130del ENSP00000385255.3:n.1046-130del
NM_001287489.1:c.1046-130del NP_001274418.1:n.1046-130del
NM_194248.2:c.1046-130del NP_919224.1:n.1046-130del
XM_005264644.2:c.1091-130del XP_005264701.1:n.1091-130del
XM_011533185.1:c.1091-130del XP_011531487.1:n.1091-130del
XM_017005338.1:c.1046-130del XP_016860827.1:n.1046-130del
NM_001287489.2:c.1046-130del NP_001274418.1:n.1046-130del
NM_194248.3:c.1046-130del MANE Select NP_919224.1:n.1046-130del
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