Canonical Allele Identifier: CA1239824177

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460205G= , CM000664.2:g.26460205G=	GRCh38
NC_000002.11:g.26683073G= , CM000664.1:g.26683073G=	GRCh37
NC_000002.10:g.26536577G=	NCBI36
NG_009937.1:g.103494C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5814C= MANE Select	ENSP00000272371.2:p.Asn1938=
ENST00000339598.8:c.3512+442C= MANE Plus Clinical	ENSP00000344521.3:n.3512+442C=
ENST00000402415.8:c.3573C=	ENSP00000383906.4:p.Asn1191=
ENST00000272371.6:c.5814C=	ENSP00000272371.2:p.Asn1938=
ENST00000338581.10:c.3513C=	ENSP00000345137.6:p.Asn1171=
ENST00000339598.7:c.3512+442C=	ENSP00000344521.3:n.3512+442C=
ENST00000402415.7:c.3744C=	ENSP00000383906.3:p.Asn1248=
ENST00000403946.7:c.5813+442C=	ENSP00000385255.3:n.5813+442C=
NM_001287489.1:c.5813+442C=	NP_001274418.1:n.5813+442C=
NM_004802.3:c.3513C=	NP_004793.2:p.Asn1171=
NM_194248.2:c.5814C=	NP_919224.1:p.Asn1938=
NM_194322.2:c.3744C=	NP_919303.1:p.Asn1248=
NM_194323.2:c.3512+442C=	NP_919304.1:n.3512+442C=
XM_005264644.2:c.5798+442C=	XP_005264701.1:n.5798+442C=
XM_011533185.1:c.5858+442C=	XP_011531487.1:n.5858+442C=
XM_017005338.1:c.5754C=	XP_016860827.1:p.Asn1918=
NM_001287489.2:c.5813+442C=	NP_001274418.1:n.5813+442C=
NM_004802.4:c.3513C=	NP_004793.2:p.Asn1171=
NM_194248.3:c.5814C= MANE Select	NP_919224.1:p.Asn1938=
NM_194322.3:c.3744C=	NP_919303.1:p.Asn1248=
NM_194323.3:c.3512+442C= MANE Plus Clinical	NP_919304.1:n.3512+442C=