Canonical Allele Identifier: CA2749240303

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26461802_26461816del , CM000664.2:g.26461802_26461816del	GRCh38
NC_000002.11:g.26684670_26684684del , CM000664.1:g.26684670_26684684del	GRCh37
NC_000002.10:g.26538174_26538188del	NCBI36
NG_009937.1:g.101887_101901del

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5417_5431del MANE Select	ENSP00000272371.2:p.Ile1806_Lys1810del
ENST00000339598.8:c.3116_3130del MANE Plus Clinical	ENSP00000344521.3:p.Ile1039_Lys1043del
ENST00000402415.8:c.3176_3190del	ENSP00000383906.4:p.Ile1059_Lys1063del
ENST00000272371.6:c.5417_5431del	ENSP00000272371.2:p.Ile1806_Lys1810del
ENST00000338581.10:c.3116_3130del	ENSP00000345137.6:p.Ile1039_Lys1043del
ENST00000339598.7:c.3116_3130del	ENSP00000344521.3:p.Ile1039_Lys1043del
ENST00000402415.7:c.3347_3361del	ENSP00000383906.3:p.Ile1116_Lys1120del
ENST00000403946.7:c.5417_5431del	ENSP00000385255.3:p.Ile1806_Lys1810del
NM_001287489.1:c.5417_5431del	NP_001274418.1:p.Ile1806_Lys1810del
NM_004802.3:c.3116_3130del	NP_004793.2:p.Ile1039_Lys1043del
NM_194248.2:c.5417_5431del	NP_919224.1:p.Ile1806_Lys1810del
NM_194322.2:c.3347_3361del	NP_919303.1:p.Ile1116_Lys1120del
NM_194323.2:c.3116_3130del	NP_919304.1:p.Ile1039_Lys1043del
XM_005264644.2:c.5402_5416del	XP_005264701.1:p.Ile1801_Lys1805del
XM_011533185.1:c.5462_5476del	XP_011531487.1:p.Ile1821_Lys1825del
XM_017005338.1:c.5357_5371del	XP_016860827.1:p.Ile1786_Lys1790del
NM_001287489.2:c.5417_5431del	NP_001274418.1:p.Ile1806_Lys1810del
NM_004802.4:c.3116_3130del	NP_004793.2:p.Ile1039_Lys1043del
NM_194248.3:c.5417_5431del MANE Select	NP_919224.1:p.Ile1806_Lys1810del
NM_194322.3:c.3347_3361del	NP_919303.1:p.Ile1116_Lys1120del
NM_194323.3:c.3116_3130del MANE Plus Clinical	NP_919304.1:p.Ile1039_Lys1043del