Canonical Allele Identifier: CA142252
Gene: OTOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21687628C>T , CM000678.2:g.21687628C>T GRCh38
NC_000016.9:g.21698949C>T , CM000678.1:g.21698949C>T GRCh37
NC_000016.8:g.21606450C>T NCBI36
NG_012973.1:g.14115C>T
NG_012973.2:g.28496C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000388958.8:c.615C>T ENSP00000373610.3:p.Arg205=
ENST00000646100.2:c.615C>T MANE Select ENSP00000496564.2:p.Arg205=
ENST00000647277.1:c.615C>T ENSP00000495594.1:p.Arg205=
ENST00000286149.8:c.615C>T ENSP00000286149.4:p.Arg205=
ENST00000388956.8:c.378C>T ENSP00000373608.4:p.Arg126=
ENST00000388958.7:c.615C>T ENSP00000373610.3:p.Arg205=
NM_001161683.1:c.378C>T NP_001155155.1:p.Arg126=
NM_144672.3:c.615C>T NP_653273.3:p.Arg205=
XM_011545747.1:c.615C>T XP_011544049.1:p.Arg205=
NM_144672.4:c.615C>T MANE Select NP_653273.3:p.Arg205=
NM_001161683.2:c.378C>T NP_001155155.1:p.Arg126=