Canonical Allele Identifier: CA346119247
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26476935C>T , CM000664.2:g.26476935C>T GRCh38
NC_000002.11:g.26699803C>T , CM000664.1:g.26699803C>T GRCh37
NC_000002.10:g.26553307C>T NCBI36
NG_009937.1:g.86764G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.2632G>A MANE Select ENSP00000272371.2:p.Glu878Lys
ENST00000339598.8:c.391G>A MANE Plus Clinical ENSP00000344521.3:p.Glu131Lys
ENST00000402415.8:c.391G>A ENSP00000383906.4:p.Glu131Lys
ENST00000272371.6:c.2632G>A ENSP00000272371.2:p.Glu878Lys
ENST00000338581.10:c.391G>A ENSP00000345137.6:p.Glu131Lys
ENST00000339598.7:c.391G>A ENSP00000344521.3:p.Glu131Lys
ENST00000402415.7:c.562G>A ENSP00000383906.3:p.Glu188Lys
ENST00000403946.7:c.2632G>A ENSP00000385255.3:p.Glu878Lys
NM_001287489.1:c.2632G>A NP_001274418.1:p.Glu878Lys
NM_004802.3:c.391G>A NP_004793.2:p.Glu131Lys
NM_194248.2:c.2632G>A NP_919224.1:p.Glu878Lys
NM_194322.2:c.562G>A NP_919303.1:p.Glu188Lys
NM_194323.2:c.391G>A NP_919304.1:p.Glu131Lys
XM_005264644.2:c.2677G>A XP_005264701.1:p.Glu893Lys
XM_011533185.1:c.2677G>A XP_011531487.1:p.Glu893Lys
XM_017005338.1:c.2632G>A XP_016860827.1:p.Glu878Lys
NM_001287489.2:c.2632G>A NP_001274418.1:p.Glu878Lys
NM_004802.4:c.391G>A NP_004793.2:p.Glu131Lys
NM_194248.3:c.2632G>A MANE Select NP_919224.1:p.Glu878Lys
NM_194322.3:c.562G>A NP_919303.1:p.Glu188Lys
NM_194323.3:c.391G>A MANE Plus Clinical NP_919304.1:p.Glu131Lys