Canonical Allele Identifier: CA2575939977

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710124dup , CM000678.2:g.21710124dup	GRCh38
NC_000016.9:g.21721445dup , CM000678.1:g.21721445dup	GRCh37
NC_000016.8:g.21628946dup	NCBI36
NG_012973.1:g.36611dup
NG_012973.2:g.50992dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1320+21dup	ENSP00000373610.3:n.1320+21dup
ENST00000646100.2:c.1320+21dup MANE Select	ENSP00000496564.2:n.1320+21dup
ENST00000647277.1:c.*134+21dup	ENSP00000495594.1:n.*134+21dup
ENST00000286149.8:c.1362+21dup	ENSP00000286149.4:n.1362+21dup
ENST00000388956.8:c.1083+21dup	ENSP00000373608.4:n.1083+21dup
ENST00000388957.3:c.348+21dup	ENSP00000373609.3:n.348+21dup
ENST00000388958.7:c.1320+21dup	ENSP00000373610.3:n.1320+21dup
ENST00000563871.5:n.540+21dup
NM_001161683.1:c.1083+21dup	NP_001155155.1:n.1083+21dup
NM_144672.3:c.1320+21dup	NP_653273.3:n.1320+21dup
NM_170664.2:c.348+21dup	NP_733764.1:n.348+21dup
XM_011545747.1:c.1320+21dup	XP_011544049.1:n.1320+21dup
XM_011545748.1:c.189+21dup	XP_011544050.1:n.189+21dup
NM_144672.4:c.1320+21dup MANE Select	NP_653273.3:n.1320+21dup
XM_011545748.2:c.189+21dup	XP_011544050.2:n.189+21dup
XR_002957775.1:n.415+21dup
NM_001161683.2:c.1083+21dup	NP_001155155.1:n.1083+21dup
NM_170664.3:c.348+21dup	NP_733764.1:n.348+21dup