Canonical Allele Identifier: CA1239816684

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26465757G= , CM000664.2:g.26465757G=	GRCh38
NC_000002.11:g.26688625G= , CM000664.1:g.26688625G=	GRCh37
NC_000002.10:g.26542129G=	NCBI36
NG_009937.1:g.97942C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.4714C= MANE Select	ENSP00000272371.2:p.Leu1572=
ENST00000339598.8:c.2413C= MANE Plus Clinical	ENSP00000344521.3:p.Leu805=
ENST00000402415.8:c.2473C=	ENSP00000383906.4:p.Leu825=
ENST00000272371.6:c.4714C=	ENSP00000272371.2:p.Leu1572=
ENST00000338581.10:c.2413C=	ENSP00000345137.6:p.Leu805=
ENST00000339598.7:c.2413C=	ENSP00000344521.3:p.Leu805=
ENST00000402415.7:c.2644C=	ENSP00000383906.3:p.Leu882=
ENST00000403946.7:c.4714C=	ENSP00000385255.3:p.Leu1572=
ENST00000464574.1:n.463C=
NM_001287489.1:c.4714C=	NP_001274418.1:p.Leu1572=
NM_004802.3:c.2413C=	NP_004793.2:p.Leu805=
NM_194248.2:c.4714C=	NP_919224.1:p.Leu1572=
NM_194322.2:c.2644C=	NP_919303.1:p.Leu882=
NM_194323.2:c.2413C=	NP_919304.1:p.Leu805=
XM_005264644.2:c.4699C=	XP_005264701.1:p.Leu1567=
XM_011533185.1:c.4759C=	XP_011531487.1:p.Leu1587=
XM_017005338.1:c.4654C=	XP_016860827.1:p.Leu1552=
NM_001287489.2:c.4714C=	NP_001274418.1:p.Leu1572=
NM_004802.4:c.2413C=	NP_004793.2:p.Leu805=
NM_194248.3:c.4714C= MANE Select	NP_919224.1:p.Leu1572=
NM_194322.3:c.2644C=	NP_919303.1:p.Leu882=
NM_194323.3:c.2413C= MANE Plus Clinical	NP_919304.1:p.Leu805=