Canonical Allele Identifier: CA1239830555

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26477801C= , CM000664.2:g.26477801C=	GRCh38
NC_000002.11:g.26700669C= , CM000664.1:g.26700669C=	GRCh37
NC_000002.10:g.26554173C=	NCBI36
NG_009937.1:g.85898G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.2215-52G= MANE Select	ENSP00000272371.2:n.2215-52G=
ENST00000339598.8:c.-28+43G= MANE Plus Clinical	ENSP00000344521.3:n.-28+43G=
ENST00000402415.8:c.-79G=	ENSP00000383906.4:n.-79G=
ENST00000272371.6:c.2215-52G=	ENSP00000272371.2:n.2215-52G=
ENST00000338581.10:c.-28+43G=	ENSP00000345137.6:n.-28+43G=
ENST00000339598.7:c.-28+43G=	ENSP00000344521.3:n.-28+43G=
ENST00000402415.7:c.93G=	ENSP00000383906.3:p.Glu31=
ENST00000403946.7:c.2215-52G=	ENSP00000385255.3:n.2215-52G=
NM_001287489.1:c.2215-52G=	NP_001274418.1:n.2215-52G=
NM_004802.3:c.-28+43G=	NP_004793.2:n.-28+43G=
NM_194248.2:c.2215-52G=	NP_919224.1:n.2215-52G=
NM_194322.2:c.93G=	NP_919303.1:p.Glu31=
NM_194323.2:c.-28+43G=	NP_919304.1:n.-28+43G=
XM_005264644.2:c.2260-52G=	XP_005264701.1:n.2260-52G=
XM_011533185.1:c.2260-52G=	XP_011531487.1:n.2260-52G=
XM_017005338.1:c.2215-52G=	XP_016860827.1:n.2215-52G=
NM_001287489.2:c.2215-52G=	NP_001274418.1:n.2215-52G=
NM_004802.4:c.-28+43G=	NP_004793.2:n.-28+43G=
NM_194248.3:c.2215-52G= MANE Select	NP_919224.1:n.2215-52G=
NM_194322.3:c.93G=	NP_919303.1:p.Glu31=
NM_194323.3:c.-28+43G= MANE Plus Clinical	NP_919304.1:n.-28+43G=