Canonical Allele Identifier: CA1239830461
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26477731T= , CM000664.2:g.26477731T= GRCh38
NC_000002.11:g.26700599T= , CM000664.1:g.26700599T= GRCh37
NC_000002.10:g.26554103T= NCBI36
NG_009937.1:g.85968A=

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.2233A= MANE Select ENSP00000272371.2:p.Ile745=
ENST00000339598.8:c.-9A= MANE Plus Clinical ENSP00000344521.3:n.-9A=
ENST00000402415.8:c.-9A= ENSP00000383906.4:n.-9A=
ENST00000272371.6:c.2233A= ENSP00000272371.2:p.Ile745=
ENST00000338581.10:c.-9A= ENSP00000345137.6:n.-9A=
ENST00000339598.7:c.-9A= ENSP00000344521.3:n.-9A=
ENST00000402415.7:c.163A= ENSP00000383906.3:p.Ile55=
ENST00000403946.7:c.2233A= ENSP00000385255.3:p.Ile745=
NM_001287489.1:c.2233A= NP_001274418.1:p.Ile745=
NM_004802.3:c.-9A= NP_004793.2:n.-9A=
NM_194248.2:c.2233A= NP_919224.1:p.Ile745=
NM_194322.2:c.163A= NP_919303.1:p.Ile55=
NM_194323.2:c.-9A= NP_919304.1:n.-9A=
XM_005264644.2:c.2278A= XP_005264701.1:p.Ile760=
XM_011533185.1:c.2278A= XP_011531487.1:p.Ile760=
XM_017005338.1:c.2233A= XP_016860827.1:p.Ile745=
NM_001287489.2:c.2233A= NP_001274418.1:p.Ile745=
NM_004802.4:c.-9A= NP_004793.2:n.-9A=
NM_194248.3:c.2233A= MANE Select NP_919224.1:p.Ile745=
NM_194322.3:c.163A= NP_919303.1:p.Ile55=
NM_194323.3:c.-9A= MANE Plus Clinical NP_919304.1:n.-9A=