Canonical Allele Identifier: CA2658237121

Gene: OTOF

Linked Data

• gnomAD v4: 2-26475929-CTGAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26475934_26475937del , CM000664.2:g.26475934_26475937del	GRCh38
NC_000002.11:g.26698802_26698805del , CM000664.1:g.26698802_26698805del	GRCh37
NC_000002.10:g.26552306_26552309del	NCBI36
NG_009937.1:g.87766_87769del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.2972_2975del MANE Select	ENSP00000272371.2:p.Asn991ArgfsTer8
ENST00000339598.8:c.731_734del MANE Plus Clinical	ENSP00000344521.3:p.Asn244ArgfsTer8
ENST00000402415.8:c.731_734del	ENSP00000383906.4:p.Asn244ArgfsTer8
ENST00000272371.6:c.2972_2975del	ENSP00000272371.2:p.Asn991ArgfsTer8
ENST00000338581.10:c.731_734del	ENSP00000345137.6:p.Asn244ArgfsTer8
ENST00000339598.7:c.731_734del	ENSP00000344521.3:p.Asn244ArgfsTer8
ENST00000402415.7:c.902_905del	ENSP00000383906.3:p.Asn301ArgfsTer8
ENST00000403946.7:c.2972_2975del	ENSP00000385255.3:p.Asn991ArgfsTer8
NM_001287489.1:c.2972_2975del	NP_001274418.1:p.Asn991ArgfsTer8
NM_004802.3:c.731_734del	NP_004793.2:p.Asn244ArgfsTer8
NM_194248.2:c.2972_2975del	NP_919224.1:p.Asn991ArgfsTer8
NM_194322.2:c.902_905del	NP_919303.1:p.Asn301ArgfsTer8
NM_194323.2:c.731_734del	NP_919304.1:p.Asn244ArgfsTer8
XM_005264644.2:c.3017_3020del	XP_005264701.1:p.Asn1006ArgfsTer8
XM_011533185.1:c.3017_3020del	XP_011531487.1:p.Asn1006ArgfsTer8
XM_017005338.1:c.2972_2975del	XP_016860827.1:p.Asn991ArgfsTer8
NM_001287489.2:c.2972_2975del	NP_001274418.1:p.Asn991ArgfsTer8
NM_004802.4:c.731_734del	NP_004793.2:p.Asn244ArgfsTer8
NM_194248.3:c.2972_2975del MANE Select	NP_919224.1:p.Asn991ArgfsTer8
NM_194322.3:c.902_905del	NP_919303.1:p.Asn301ArgfsTer8
NM_194323.3:c.731_734del MANE Plus Clinical	NP_919304.1:p.Asn244ArgfsTer8