Canonical Allele Identifier: CA1239825436
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26461804A= , CM000664.2:g.26461804A= GRCh38
NC_000002.11:g.26684672A= , CM000664.1:g.26684672A= GRCh37
NC_000002.10:g.26538176A= NCBI36
NG_009937.1:g.101895T=

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.5425T= MANE Select ENSP00000272371.2:p.Ser1809=
ENST00000339598.8:c.3124T= MANE Plus Clinical ENSP00000344521.3:p.Ser1042=
ENST00000402415.8:c.3184T= ENSP00000383906.4:p.Ser1062=
ENST00000272371.6:c.5425T= ENSP00000272371.2:p.Ser1809=
ENST00000338581.10:c.3124T= ENSP00000345137.6:p.Ser1042=
ENST00000339598.7:c.3124T= ENSP00000344521.3:p.Ser1042=
ENST00000402415.7:c.3355T= ENSP00000383906.3:p.Ser1119=
ENST00000403946.7:c.5425T= ENSP00000385255.3:p.Ser1809=
NM_001287489.1:c.5425T= NP_001274418.1:p.Ser1809=
NM_004802.3:c.3124T= NP_004793.2:p.Ser1042=
NM_194248.2:c.5425T= NP_919224.1:p.Ser1809=
NM_194322.2:c.3355T= NP_919303.1:p.Ser1119=
NM_194323.2:c.3124T= NP_919304.1:p.Ser1042=
XM_005264644.2:c.5410T= XP_005264701.1:p.Ser1804=
XM_011533185.1:c.5470T= XP_011531487.1:p.Ser1824=
XM_017005338.1:c.5365T= XP_016860827.1:p.Ser1789=
NM_001287489.2:c.5425T= NP_001274418.1:p.Ser1809=
NM_004802.4:c.3124T= NP_004793.2:p.Ser1042=
NM_194248.3:c.5425T= MANE Select NP_919224.1:p.Ser1809=
NM_194322.3:c.3355T= NP_919303.1:p.Ser1119=
NM_194323.3:c.3124T= MANE Plus Clinical NP_919304.1:p.Ser1042=