Canonical Allele Identifier: CA1239818507

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467448_26467451delinsTCTC , CM000664.2:g.26467448_26467451delinsTCTC	GRCh38
NC_000002.11:g.26690316_26690319delinsTCTC , CM000664.1:g.26690316_26690319delinsTCTC	GRCh37
NC_000002.10:g.26543820_26543823delinsTCTC	NCBI36
NG_009937.1:g.96248_96251delinsGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4141_4144delinsGAGA MANE Select	ENSP00000272371.2:p.Glu1381=
ENST00000339598.8:c.1840_1843delinsGAGA MANE Plus Clinical	ENSP00000344521.3:p.Glu614=
ENST00000402415.8:c.1900_1903delinsGAGA	ENSP00000383906.4:p.Glu634=
ENST00000272371.6:c.4141_4144delinsGAGA	ENSP00000272371.2:p.Glu1381=
ENST00000338581.10:c.1840_1843delinsGAGA	ENSP00000345137.6:p.Glu614=
ENST00000339598.7:c.1840_1843delinsGAGA	ENSP00000344521.3:p.Glu614=
ENST00000402415.7:c.2071_2074delinsGAGA	ENSP00000383906.3:p.Glu691=
ENST00000403946.7:c.4141_4144delinsGAGA	ENSP00000385255.3:p.Glu1381=
NM_001287489.1:c.4141_4144delinsGAGA	NP_001274418.1:p.Glu1381=
NM_004802.3:c.1840_1843delinsGAGA	NP_004793.2:p.Glu614=
NM_194248.2:c.4141_4144delinsGAGA	NP_919224.1:p.Glu1381=
NM_194322.2:c.2071_2074delinsGAGA	NP_919303.1:p.Glu691=
NM_194323.2:c.1840_1843delinsGAGA	NP_919304.1:p.Glu614=
XM_005264644.2:c.4126_4129delinsGAGA	XP_005264701.1:p.Glu1376=
XM_011533185.1:c.4186_4189delinsGAGA	XP_011531487.1:p.Glu1396=
XM_017005338.1:c.4081_4084delinsGAGA	XP_016860827.1:p.Glu1361=
NM_001287489.2:c.4141_4144delinsGAGA	NP_001274418.1:p.Glu1381=
NM_004802.4:c.1840_1843delinsGAGA	NP_004793.2:p.Glu614=
NM_194248.3:c.4141_4144delinsGAGA MANE Select	NP_919224.1:p.Glu1381=
NM_194322.3:c.2071_2074delinsGAGA	NP_919303.1:p.Glu691=
NM_194323.3:c.1840_1843delinsGAGA MANE Plus Clinical	NP_919304.1:p.Glu614=