Canonical Allele Identifier: CA1239831549
Gene: OTOF HGNC NCBI

Linked Data

dbSNP Id: rs1665659251
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26484689A>T , CM000664.2:g.26484689A>T GRCh38
NC_000002.11:g.26707557A>T , CM000664.1:g.26707557A>T GRCh37
NC_000002.10:g.26561061A>T NCBI36
NG_009937.1:g.79010T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1046-56T>A MANE Select ENSP00000272371.2:n.1046-56T>A
ENST00000272371.6:c.1046-56T>A ENSP00000272371.2:n.1046-56T>A
ENST00000403946.7:c.1046-56T>A ENSP00000385255.3:n.1046-56T>A
NM_001287489.1:c.1046-56T>A NP_001274418.1:n.1046-56T>A
NM_194248.2:c.1046-56T>A NP_919224.1:n.1046-56T>A
XM_005264644.2:c.1091-56T>A XP_005264701.1:n.1091-56T>A
XM_011533185.1:c.1091-56T>A XP_011531487.1:n.1091-56T>A
XM_017005338.1:c.1046-56T>A XP_016860827.1:n.1046-56T>A
NM_001287489.2:c.1046-56T>A NP_001274418.1:n.1046-56T>A
NM_194248.3:c.1046-56T>A MANE Select NP_919224.1:n.1046-56T>A
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