Canonical Allele Identifier: CA2575940102
Gene: OTOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21722978dup , CM000678.2:g.21722978dup GRCh38
NC_000016.9:g.21734299dup , CM000678.1:g.21734299dup GRCh37
NC_000016.8:g.21641800dup NCBI36
NG_012973.1:g.49465dup
NG_012973.2:g.63846dup

Transcript Alleles

HGVS Amino-acid change
ENST00000388958.8:c.1880dup ENSP00000373610.3:p.Ala628GlyfsTer?
ENST00000646100.2:c.1880dup MANE Select ENSP00000496564.2:p.Ala628GlyfsTer?
ENST00000647277.1:c.*694dup ENSP00000495594.1:n.*694dup
ENST00000286149.8:c.1922dup ENSP00000286149.4:p.Ala642GlyfsTer?
ENST00000388956.8:c.1643dup ENSP00000373608.4:p.Ala549GlyfsTer?
ENST00000388957.3:c.908dup ENSP00000373609.3:p.Ala304GlyfsTer?
ENST00000388958.7:c.1880dup ENSP00000373610.3:p.Ala628GlyfsTer?
ENST00000563871.5:n.1295dup
NM_001161683.1:c.1643dup NP_001155155.1:p.Ala549GlyfsTer?
NM_144672.3:c.1880dup NP_653273.3:p.Ala628GlyfsTer?
NM_170664.2:c.908dup NP_733764.1:p.Ala304GlyfsTer?
XM_011545747.1:c.1880dup XP_011544049.1:p.Ala628GlyfsTer?
XM_011545748.1:c.749dup XP_011544050.1:p.Ala251GlyfsTer?
NM_144672.4:c.1880dup MANE Select NP_653273.3:p.Ala628GlyfsTer?
XM_011545748.2:c.749dup XP_011544050.2:p.Ala251GlyfsTer?
XM_017022951.1:c.146dup XP_016878440.1:p.Ala50GlyfsTer?
XR_002957775.1:n.975dup
NM_001161683.2:c.1643dup NP_001155155.1:p.Ala549GlyfsTer?
NM_170664.3:c.908dup NP_733764.1:p.Ala304GlyfsTer?