Canonical Allele Identifier: CA1239829695
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26477213A= , CM000664.2:g.26477213A= GRCh38
NC_000002.11:g.26700081A= , CM000664.1:g.26700081A= GRCh37
NC_000002.10:g.26553585A= NCBI36
NG_009937.1:g.86486T=

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.2482T= MANE Select ENSP00000272371.2:p.Cys828=
ENST00000339598.8:c.241T= MANE Plus Clinical ENSP00000344521.3:p.Cys81=
ENST00000402415.8:c.241T= ENSP00000383906.4:p.Cys81=
ENST00000272371.6:c.2482T= ENSP00000272371.2:p.Cys828=
ENST00000338581.10:c.241T= ENSP00000345137.6:p.Cys81=
ENST00000339598.7:c.241T= ENSP00000344521.3:p.Cys81=
ENST00000402415.7:c.412T= ENSP00000383906.3:p.Cys138=
ENST00000403946.7:c.2482T= ENSP00000385255.3:p.Cys828=
NM_001287489.1:c.2482T= NP_001274418.1:p.Cys828=
NM_004802.3:c.241T= NP_004793.2:p.Cys81=
NM_194248.2:c.2482T= NP_919224.1:p.Cys828=
NM_194322.2:c.412T= NP_919303.1:p.Cys138=
NM_194323.2:c.241T= NP_919304.1:p.Cys81=
XM_005264644.2:c.2527T= XP_005264701.1:p.Cys843=
XM_011533185.1:c.2527T= XP_011531487.1:p.Cys843=
XM_017005338.1:c.2482T= XP_016860827.1:p.Cys828=
NM_001287489.2:c.2482T= NP_001274418.1:p.Cys828=
NM_004802.4:c.241T= NP_004793.2:p.Cys81=
NM_194248.3:c.2482T= MANE Select NP_919224.1:p.Cys828=
NM_194322.3:c.412T= NP_919303.1:p.Cys138=
NM_194323.3:c.241T= MANE Plus Clinical NP_919304.1:p.Cys81=