Canonical Allele Identifier: CA1239817541

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26466731G= , CM000664.2:g.26466731G=	GRCh38
NC_000002.11:g.26689599G= , CM000664.1:g.26689599G=	GRCh37
NC_000002.10:g.26543103G=	NCBI36
NG_009937.1:g.96968C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4483C= MANE Select	ENSP00000272371.2:p.Arg1495=
ENST00000339598.8:c.2182C= MANE Plus Clinical	ENSP00000344521.3:p.Arg728=
ENST00000402415.8:c.2242C=	ENSP00000383906.4:p.Arg748=
ENST00000272371.6:c.4483C=	ENSP00000272371.2:p.Arg1495=
ENST00000338581.10:c.2182C=	ENSP00000345137.6:p.Arg728=
ENST00000339598.7:c.2182C=	ENSP00000344521.3:p.Arg728=
ENST00000402415.7:c.2413C=	ENSP00000383906.3:p.Arg805=
ENST00000403946.7:c.4483C=	ENSP00000385255.3:p.Arg1495=
NM_001287489.1:c.4483C=	NP_001274418.1:p.Arg1495=
NM_004802.3:c.2182C=	NP_004793.2:p.Arg728=
NM_194248.2:c.4483C=	NP_919224.1:p.Arg1495=
NM_194322.2:c.2413C=	NP_919303.1:p.Arg805=
NM_194323.2:c.2182C=	NP_919304.1:p.Arg728=
XM_005264644.2:c.4468C=	XP_005264701.1:p.Arg1490=
XM_011533185.1:c.4528C=	XP_011531487.1:p.Arg1510=
XM_017005338.1:c.4423C=	XP_016860827.1:p.Arg1475=
NM_001287489.2:c.4483C=	NP_001274418.1:p.Arg1495=
NM_004802.4:c.2182C=	NP_004793.2:p.Arg728=
NM_194248.3:c.4483C= MANE Select	NP_919224.1:p.Arg1495=
NM_194322.3:c.2413C=	NP_919303.1:p.Arg805=
NM_194323.3:c.2182C= MANE Plus Clinical	NP_919304.1:p.Arg728=