Canonical Allele Identifier: CA1239822009
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26457994G= , CM000664.2:g.26457994G= GRCh38
NC_000002.11:g.26680862G= , CM000664.1:g.26680862G= GRCh37
NC_000002.10:g.26534366G= NCBI36
NG_009937.1:g.105705C=
NG_042824.1:g.61083G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.*244C= MANE Select ENSP00000272371.2:n.*244C=
ENST00000339598.8:c.*46C= MANE Plus Clinical ENSP00000344521.3:n.*46C=
ENST00000402415.8:c.*244C= ENSP00000383906.4:n.*244C=
ENST00000272371.6:c.*244C= ENSP00000272371.2:n.*244C=
ENST00000338581.10:c.*244C= ENSP00000345137.6:n.*244C=
ENST00000339598.7:c.*46C= ENSP00000344521.3:n.*46C=
ENST00000402415.7:c.*244C= ENSP00000383906.3:n.*244C=
ENST00000403946.7:c.*46C= ENSP00000385255.3:n.*46C=
NM_001287489.1:c.*46C= NP_001274418.1:n.*46C=
NM_004802.3:c.*244C= NP_004793.2:n.*244C=
NM_194248.2:c.*244C= NP_919224.1:n.*244C=
NM_194322.2:c.*244C= NP_919303.1:n.*244C=
NM_194323.2:c.*46C= NP_919304.1:n.*46C=
XM_005264644.2:c.6025C= XP_005264701.1:n.6025C=
XM_011533185.1:c.6085C= XP_011531487.1:n.6085C=
NM_001287489.2:c.*46C= NP_001274418.1:n.*46C=
NM_004802.4:c.*244C= NP_004793.2:n.*244C=
NM_194248.3:c.*244C= MANE Select NP_919224.1:n.*244C=
NM_194322.3:c.*244C= NP_919303.1:n.*244C=
NM_194323.3:c.*46C= MANE Plus Clinical NP_919304.1:n.*46C=