Canonical Allele Identifier: CA1239822138

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26458074G= , CM000664.2:g.26458074G=	GRCh38
NC_000002.11:g.26680942G= , CM000664.1:g.26680942G=	GRCh37
NC_000002.10:g.26534446G=	NCBI36
NG_009937.1:g.105625C=
NG_042824.1:g.61163G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.*164C= MANE Select	ENSP00000272371.2:n.*164C=
ENST00000339598.8:c.3659C= MANE Plus Clinical	ENSP00000344521.3:p.Pro1220=
ENST00000402415.8:c.*164C=	ENSP00000383906.4:n.*164C=
ENST00000272371.6:c.*164C=	ENSP00000272371.2:n.*164C=
ENST00000338581.10:c.*164C=	ENSP00000345137.6:n.*164C=
ENST00000339598.7:c.3659C=	ENSP00000344521.3:p.Pro1220=
ENST00000402415.7:c.*164C=	ENSP00000383906.3:n.*164C=
ENST00000403946.7:c.5960C=	ENSP00000385255.3:p.Pro1987=
NM_001287489.1:c.5960C=	NP_001274418.1:p.Pro1987=
NM_004802.3:c.*164C=	NP_004793.2:n.*164C=
NM_194248.2:c.*164C=	NP_919224.1:n.*164C=
NM_194322.2:c.*164C=	NP_919303.1:n.*164C=
NM_194323.2:c.3659C=	NP_919304.1:p.Pro1220=
XM_005264644.2:c.5945C=	XP_005264701.1:p.Pro1982=
XM_011533185.1:c.6005C=	XP_011531487.1:p.Pro2002=
NM_001287489.2:c.5960C=	NP_001274418.1:p.Pro1987=
NM_004802.4:c.*164C=	NP_004793.2:n.*164C=
NM_194248.3:c.*164C= MANE Select	NP_919224.1:n.*164C=
NM_194322.3:c.*164C=	NP_919303.1:n.*164C=
NM_194323.3:c.3659C= MANE Plus Clinical	NP_919304.1:p.Pro1220=