Canonical Allele Identifier: CA1239824156

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460193C= , CM000664.2:g.26460193C=	GRCh38
NC_000002.11:g.26683061C= , CM000664.1:g.26683061C=	GRCh37
NC_000002.10:g.26536565C=	NCBI36
NG_009937.1:g.103506G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.5826G= MANE Select	ENSP00000272371.2:p.Thr1942=
ENST00000339598.8:c.3512+454G= MANE Plus Clinical	ENSP00000344521.3:n.3512+454G=
ENST00000402415.8:c.3585G=	ENSP00000383906.4:p.Thr1195=
ENST00000272371.6:c.5826G=	ENSP00000272371.2:p.Thr1942=
ENST00000338581.10:c.3525G=	ENSP00000345137.6:p.Thr1175=
ENST00000339598.7:c.3512+454G=	ENSP00000344521.3:n.3512+454G=
ENST00000402415.7:c.3756G=	ENSP00000383906.3:p.Thr1252=
ENST00000403946.7:c.5813+454G=	ENSP00000385255.3:n.5813+454G=
NM_001287489.1:c.5813+454G=	NP_001274418.1:n.5813+454G=
NM_004802.3:c.3525G=	NP_004793.2:p.Thr1175=
NM_194248.2:c.5826G=	NP_919224.1:p.Thr1942=
NM_194322.2:c.3756G=	NP_919303.1:p.Thr1252=
NM_194323.2:c.3512+454G=	NP_919304.1:n.3512+454G=
XM_005264644.2:c.5798+454G=	XP_005264701.1:n.5798+454G=
XM_011533185.1:c.5858+454G=	XP_011531487.1:n.5858+454G=
XM_017005338.1:c.5766G=	XP_016860827.1:p.Thr1922=
NM_001287489.2:c.5813+454G=	NP_001274418.1:n.5813+454G=
NM_004802.4:c.3525G=	NP_004793.2:p.Thr1175=
NM_194248.3:c.5826G= MANE Select	NP_919224.1:p.Thr1942=
NM_194322.3:c.3756G=	NP_919303.1:p.Thr1252=
NM_194323.3:c.3512+454G= MANE Plus Clinical	NP_919304.1:n.3512+454G=