Canonical Allele Identifier: CA1239825485
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26461906C= , CM000664.2:g.26461906C= GRCh38
NC_000002.11:g.26684774C= , CM000664.1:g.26684774C= GRCh37
NC_000002.10:g.26538278C= NCBI36
NG_009937.1:g.101793G=

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.5323G= MANE Select ENSP00000272371.2:p.Asp1775=
ENST00000339598.8:c.3022G= MANE Plus Clinical ENSP00000344521.3:p.Asp1008=
ENST00000402415.8:c.3082G= ENSP00000383906.4:p.Asp1028=
ENST00000272371.6:c.5323G= ENSP00000272371.2:p.Asp1775=
ENST00000338581.10:c.3022G= ENSP00000345137.6:p.Asp1008=
ENST00000339598.7:c.3022G= ENSP00000344521.3:p.Asp1008=
ENST00000402415.7:c.3253G= ENSP00000383906.3:p.Asp1085=
ENST00000403946.7:c.5323G= ENSP00000385255.3:p.Asp1775=
NM_001287489.1:c.5323G= NP_001274418.1:p.Asp1775=
NM_004802.3:c.3022G= NP_004793.2:p.Asp1008=
NM_194248.2:c.5323G= NP_919224.1:p.Asp1775=
NM_194322.2:c.3253G= NP_919303.1:p.Asp1085=
NM_194323.2:c.3022G= NP_919304.1:p.Asp1008=
XM_005264644.2:c.5308G= XP_005264701.1:p.Asp1770=
XM_011533185.1:c.5368G= XP_011531487.1:p.Asp1790=
XM_017005338.1:c.5263G= XP_016860827.1:p.Asp1755=
NM_001287489.2:c.5323G= NP_001274418.1:p.Asp1775=
NM_004802.4:c.3022G= NP_004793.2:p.Asp1008=
NM_194248.3:c.5323G= MANE Select NP_919224.1:p.Asp1775=
NM_194322.3:c.3253G= NP_919303.1:p.Asp1085=
NM_194323.3:c.3022G= MANE Plus Clinical NP_919304.1:p.Asp1008=