Canonical Allele Identifier: CA1239818422

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467372T= , CM000664.2:g.26467372T=	GRCh38
NC_000002.11:g.26690240T= , CM000664.1:g.26690240T=	GRCh37
NC_000002.10:g.26543744T=	NCBI36
NG_009937.1:g.96327A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4220A= MANE Select	ENSP00000272371.2:p.Glu1407=
ENST00000339598.8:c.1919A= MANE Plus Clinical	ENSP00000344521.3:p.Glu640=
ENST00000402415.8:c.1979A=	ENSP00000383906.4:p.Glu660=
ENST00000272371.6:c.4220A=	ENSP00000272371.2:p.Glu1407=
ENST00000338581.10:c.1919A=	ENSP00000345137.6:p.Glu640=
ENST00000339598.7:c.1919A=	ENSP00000344521.3:p.Glu640=
ENST00000402415.7:c.2150A=	ENSP00000383906.3:p.Glu717=
ENST00000403946.7:c.4220A=	ENSP00000385255.3:p.Glu1407=
NM_001287489.1:c.4220A=	NP_001274418.1:p.Glu1407=
NM_004802.3:c.1919A=	NP_004793.2:p.Glu640=
NM_194248.2:c.4220A=	NP_919224.1:p.Glu1407=
NM_194322.2:c.2150A=	NP_919303.1:p.Glu717=
NM_194323.2:c.1919A=	NP_919304.1:p.Glu640=
XM_005264644.2:c.4205A=	XP_005264701.1:p.Glu1402=
XM_011533185.1:c.4265A=	XP_011531487.1:p.Glu1422=
XM_017005338.1:c.4160A=	XP_016860827.1:p.Glu1387=
NM_001287489.2:c.4220A=	NP_001274418.1:p.Glu1407=
NM_004802.4:c.1919A=	NP_004793.2:p.Glu640=
NM_194248.3:c.4220A= MANE Select	NP_919224.1:p.Glu1407=
NM_194322.3:c.2150A=	NP_919303.1:p.Glu717=
NM_194323.3:c.1919A= MANE Plus Clinical	NP_919304.1:p.Glu640=