Canonical Allele Identifier: CA1239816578
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26465677G= , CM000664.2:g.26465677G= GRCh38
NC_000002.11:g.26688545G= , CM000664.1:g.26688545G= GRCh37
NC_000002.10:g.26542049G= NCBI36
NG_009937.1:g.98022C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.4794C= MANE Select ENSP00000272371.2:p.Tyr1598=
ENST00000339598.8:c.2493C= MANE Plus Clinical ENSP00000344521.3:p.Tyr831=
ENST00000402415.8:c.2553C= ENSP00000383906.4:p.Tyr851=
ENST00000272371.6:c.4794C= ENSP00000272371.2:p.Tyr1598=
ENST00000338581.10:c.2493C= ENSP00000345137.6:p.Tyr831=
ENST00000339598.7:c.2493C= ENSP00000344521.3:p.Tyr831=
ENST00000402415.7:c.2724C= ENSP00000383906.3:p.Tyr908=
ENST00000403946.7:c.4794C= ENSP00000385255.3:p.Tyr1598=
ENST00000464574.1:n.543C=
NM_001287489.1:c.4794C= NP_001274418.1:p.Tyr1598=
NM_004802.3:c.2493C= NP_004793.2:p.Tyr831=
NM_194248.2:c.4794C= NP_919224.1:p.Tyr1598=
NM_194322.2:c.2724C= NP_919303.1:p.Tyr908=
NM_194323.2:c.2493C= NP_919304.1:p.Tyr831=
XM_005264644.2:c.4779C= XP_005264701.1:p.Tyr1593=
XM_011533185.1:c.4839C= XP_011531487.1:p.Tyr1613=
XM_017005338.1:c.4734C= XP_016860827.1:p.Tyr1578=
NM_001287489.2:c.4794C= NP_001274418.1:p.Tyr1598=
NM_004802.4:c.2493C= NP_004793.2:p.Tyr831=
NM_194248.3:c.4794C= MANE Select NP_919224.1:p.Tyr1598=
NM_194322.3:c.2724C= NP_919303.1:p.Tyr908=
NM_194323.3:c.2493C= MANE Plus Clinical NP_919304.1:p.Tyr831=