Canonical Allele Identifier: CA2212563245
Gene: OTOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21709860C= , CM000678.2:g.21709860C= GRCh38
NC_000016.9:g.21721181C= , CM000678.1:g.21721181C= GRCh37
NC_000016.8:g.21628682C= NCBI36
NG_012973.1:g.36347C=
NG_012973.2:g.50728C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000388958.8:c.1105-28C= ENSP00000373610.3:n.1105-28C=
ENST00000646100.2:c.1105-28C= MANE Select ENSP00000496564.2:n.1105-28C=
ENST00000647277.1:c.981-28C= ENSP00000495594.1:n.981-28C=
ENST00000286149.8:c.1147-28C= ENSP00000286149.4:n.1147-28C=
ENST00000388956.8:c.868-28C= ENSP00000373608.4:n.868-28C=
ENST00000388957.3:c.133-28C= ENSP00000373609.3:n.133-28C=
ENST00000388958.7:c.1105-28C= ENSP00000373610.3:n.1105-28C=
ENST00000563871.5:n.325-28C=
ENST00000569064.1:n.479-28C=
NM_001161683.1:c.868-28C= NP_001155155.1:n.868-28C=
NM_144672.3:c.1105-28C= NP_653273.3:n.1105-28C=
NM_170664.2:c.133-28C= NP_733764.1:n.133-28C=
XM_011545747.1:c.1105-28C= XP_011544049.1:n.1105-28C=
XM_011545748.1:c.-27-28C= XP_011544050.1:n.-27-28C=
NM_144672.4:c.1105-28C= MANE Select NP_653273.3:n.1105-28C=
XM_011545748.2:c.-27-28C= XP_011544050.2:n.-27-28C=
XR_002957775.1:n.200-28C=
NM_001161683.2:c.868-28C= NP_001155155.1:n.868-28C=
NM_170664.3:c.133-28C= NP_733764.1:n.133-28C=