Canonical Allele Identifier: CA2632220240

Gene: OTOA

Linked Data

• gnomAD v4: 16-21710155-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710157del , CM000678.2:g.21710157del	GRCh38
NC_000016.9:g.21721478del , CM000678.1:g.21721478del	GRCh37
NC_000016.8:g.21628979del	NCBI36
NG_012973.1:g.36644del
NG_012973.2:g.51025del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1320+54del	ENSP00000373610.3:n.1320+54del
ENST00000646100.2:c.1320+54del MANE Select	ENSP00000496564.2:n.1320+54del
ENST00000647277.1:c.*134+54del	ENSP00000495594.1:n.*134+54del
ENST00000286149.8:c.1362+54del	ENSP00000286149.4:n.1362+54del
ENST00000388956.8:c.1083+54del	ENSP00000373608.4:n.1083+54del
ENST00000388957.3:c.348+54del	ENSP00000373609.3:n.348+54del
ENST00000388958.7:c.1320+54del	ENSP00000373610.3:n.1320+54del
ENST00000563871.5:n.540+54del
NM_001161683.1:c.1083+54del	NP_001155155.1:n.1083+54del
NM_144672.3:c.1320+54del	NP_653273.3:n.1320+54del
NM_170664.2:c.348+54del	NP_733764.1:n.348+54del
XM_011545747.1:c.1320+54del	XP_011544049.1:n.1320+54del
XM_011545748.1:c.189+54del	XP_011544050.1:n.189+54del
NM_144672.4:c.1320+54del MANE Select	NP_653273.3:n.1320+54del
XM_011545748.2:c.189+54del	XP_011544050.2:n.189+54del
XR_002957775.1:n.415+54del
NM_001161683.2:c.1083+54del	NP_001155155.1:n.1083+54del
NM_170664.3:c.348+54del	NP_733764.1:n.348+54del