Canonical Allele Identifier: CA1239831228

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26484490C= , CM000664.2:g.26484490C=	GRCh38
NC_000002.11:g.26707358C= , CM000664.1:g.26707358C=	GRCh37
NC_000002.10:g.26560862C=	NCBI36
NG_009937.1:g.79209G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.1189G= MANE Select	ENSP00000272371.2:p.Glu397=
ENST00000272371.6:c.1189G=	ENSP00000272371.2:p.Glu397=
ENST00000403946.7:c.1189G=	ENSP00000385255.3:p.Glu397=
NM_001287489.1:c.1189G=	NP_001274418.1:p.Glu397=
NM_194248.2:c.1189G=	NP_919224.1:p.Glu397=
XM_005264644.2:c.1234G=	XP_005264701.1:p.Glu412=
XM_011533185.1:c.1234G=	XP_011531487.1:p.Glu412=
XM_017005338.1:c.1189G=	XP_016860827.1:p.Glu397=
NM_001287489.2:c.1189G=	NP_001274418.1:p.Glu397=
NM_194248.3:c.1189G= MANE Select	NP_919224.1:p.Glu397=