Canonical Allele Identifier: CA1239830050

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26477420_26477421delinsTC , CM000664.2:g.26477420_26477421delinsTC	GRCh38
NC_000002.11:g.26700288_26700289delinsTC , CM000664.1:g.26700288_26700289delinsTC	GRCh37
NC_000002.10:g.26553792_26553793delinsTC	NCBI36
NG_009937.1:g.86278_86279delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.2401_2402delinsGA MANE Select	ENSP00000272371.2:p.Glu801=
ENST00000339598.8:c.160_161delinsGA MANE Plus Clinical	ENSP00000344521.3:p.Glu54=
ENST00000402415.8:c.160_161delinsGA	ENSP00000383906.4:p.Glu54=
ENST00000272371.6:c.2401_2402delinsGA	ENSP00000272371.2:p.Glu801=
ENST00000338581.10:c.160_161delinsGA	ENSP00000345137.6:p.Glu54=
ENST00000339598.7:c.160_161delinsGA	ENSP00000344521.3:p.Glu54=
ENST00000402415.7:c.331_332delinsGA	ENSP00000383906.3:p.Glu111=
ENST00000403946.7:c.2401_2402delinsGA	ENSP00000385255.3:p.Glu801=
NM_001287489.1:c.2401_2402delinsGA	NP_001274418.1:p.Glu801=
NM_004802.3:c.160_161delinsGA	NP_004793.2:p.Glu54=
NM_194248.2:c.2401_2402delinsGA	NP_919224.1:p.Glu801=
NM_194322.2:c.331_332delinsGA	NP_919303.1:p.Glu111=
NM_194323.2:c.160_161delinsGA	NP_919304.1:p.Glu54=
XM_005264644.2:c.2446_2447delinsGA	XP_005264701.1:p.Glu816=
XM_011533185.1:c.2446_2447delinsGA	XP_011531487.1:p.Glu816=
XM_017005338.1:c.2401_2402delinsGA	XP_016860827.1:p.Glu801=
NM_001287489.2:c.2401_2402delinsGA	NP_001274418.1:p.Glu801=
NM_004802.4:c.160_161delinsGA	NP_004793.2:p.Glu54=
NM_194248.3:c.2401_2402delinsGA MANE Select	NP_919224.1:p.Glu801=
NM_194322.3:c.331_332delinsGA	NP_919303.1:p.Glu111=
NM_194323.3:c.160_161delinsGA MANE Plus Clinical	NP_919304.1:p.Glu54=