Canonical Allele Identifier: CA1239827738
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26475974G= , CM000664.2:g.26475974G= GRCh38
NC_000002.11:g.26698842G= , CM000664.1:g.26698842G= GRCh37
NC_000002.10:g.26552346G= NCBI36
NG_009937.1:g.87725C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.2931C= MANE Select ENSP00000272371.2:p.Ser977=
ENST00000339598.8:c.690C= MANE Plus Clinical ENSP00000344521.3:p.Ser230=
ENST00000402415.8:c.690C= ENSP00000383906.4:p.Ser230=
ENST00000272371.6:c.2931C= ENSP00000272371.2:p.Ser977=
ENST00000338581.10:c.690C= ENSP00000345137.6:p.Ser230=
ENST00000339598.7:c.690C= ENSP00000344521.3:p.Ser230=
ENST00000402415.7:c.861C= ENSP00000383906.3:p.Ser287=
ENST00000403946.7:c.2931C= ENSP00000385255.3:p.Ser977=
NM_001287489.1:c.2931C= NP_001274418.1:p.Ser977=
NM_004802.3:c.690C= NP_004793.2:p.Ser230=
NM_194248.2:c.2931C= NP_919224.1:p.Ser977=
NM_194322.2:c.861C= NP_919303.1:p.Ser287=
NM_194323.2:c.690C= NP_919304.1:p.Ser230=
XM_005264644.2:c.2976C= XP_005264701.1:p.Ser992=
XM_011533185.1:c.2976C= XP_011531487.1:p.Ser992=
XM_017005338.1:c.2931C= XP_016860827.1:p.Ser977=
NM_001287489.2:c.2931C= NP_001274418.1:p.Ser977=
NM_004802.4:c.690C= NP_004793.2:p.Ser230=
NM_194248.3:c.2931C= MANE Select NP_919224.1:p.Ser977=
NM_194322.3:c.861C= NP_919303.1:p.Ser287=
NM_194323.3:c.690C= MANE Plus Clinical NP_919304.1:p.Ser230=