Canonical Allele Identifier: CA1239829407
Gene: OTOF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482757G= , CM000664.2:g.26482757G= GRCh38
NC_000002.11:g.26705625G= , CM000664.1:g.26705625G= GRCh37
NC_000002.10:g.26559129G= NCBI36
NG_009937.1:g.80942C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-165C= MANE Select ENSP00000272371.2:n.1393-165C=
ENST00000272371.6:c.1393-165C= ENSP00000272371.2:n.1393-165C=
ENST00000403946.7:c.1393-165C= ENSP00000385255.3:n.1393-165C=
NM_001287489.1:c.1393-165C= NP_001274418.1:n.1393-165C=
NM_194248.2:c.1393-165C= NP_919224.1:n.1393-165C=
XM_005264644.2:c.1438-165C= XP_005264701.1:n.1438-165C=
XM_011533185.1:c.1438-165C= XP_011531487.1:n.1438-165C=
XM_017005338.1:c.1393-165C= XP_016860827.1:n.1393-165C=
NM_001287489.2:c.1393-165C= NP_001274418.1:n.1393-165C=
NM_194248.3:c.1393-165C= MANE Select NP_919224.1:n.1393-165C=
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