Canonical Allele Identifier: CA1239825483

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26461897C= , CM000664.2:g.26461897C=	GRCh38
NC_000002.11:g.26684765C= , CM000664.1:g.26684765C=	GRCh37
NC_000002.10:g.26538269C=	NCBI36
NG_009937.1:g.101802G=

Transcript Alleles

HGVS	Amino-acid Change
NM_194248.3:c.5332G= MANE Select	NP_919224.1:p.Val1778=
ENST00000272371.7:c.5332G= MANE Select	ENSP00000272371.2:p.Val1778=
NM_194323.3:c.3031G= MANE Plus Clinical	NP_919304.1:p.Val1011=
ENST00000339598.8:c.3031G= MANE Plus Clinical	ENSP00000344521.3:p.Val1011=
NM_001287489.1:c.5332G=	NP_001274418.1:p.Val1778=
NM_001287489.2:c.5332G=	NP_001274418.1:p.Val1778=
NM_004802.3:c.3031G=	NP_004793.2:p.Val1011=
NM_004802.4:c.3031G=	NP_004793.2:p.Val1011=
NM_194248.2:c.5332G=	NP_919224.1:p.Val1778=
NM_194322.2:c.3262G=	NP_919303.1:p.Val1088=
NM_194322.3:c.3262G=	NP_919303.1:p.Val1088=
NM_194323.2:c.3031G=	NP_919304.1:p.Val1011=
ENST00000272371.6:c.5332G=	ENSP00000272371.2:p.Val1778=
ENST00000338581.10:c.3031G=	ENSP00000345137.6:p.Val1011=
ENST00000339598.7:c.3031G=	ENSP00000344521.3:p.Val1011=
ENST00000402415.7:c.3262G=	ENSP00000383906.3:p.Val1088=
ENST00000402415.8:c.3091G=	ENSP00000383906.4:p.Val1031=
ENST00000403946.7:c.5332G=	ENSP00000385255.3:p.Val1778=
XM_005264644.2:c.5317G=	XP_005264701.1:p.Val1773=
XM_011533185.1:c.5377G=	XP_011531487.1:p.Val1793=
XM_017005338.1:c.5272G=	XP_016860827.1:p.Val1758=