Canonical Allele Identifier: CA2212553010
Gene: OTOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21736226T= , CM000678.2:g.21736226T= GRCh38
NC_000016.9:g.21747547T= , CM000678.1:g.21747547T= GRCh37
NC_000016.8:g.21655048T= NCBI36
NG_012973.1:g.62713T=
NG_012973.2:g.77094T=

Transcript Alleles

HGVS Amino-acid change
ENST00000388958.8:c.2302-35T= ENSP00000373610.3:n.2302-35T=
ENST00000646100.2:c.2302-35T= MANE Select ENSP00000496564.2:n.2302-35T=
ENST00000647277.1:c.*1116-35T= ENSP00000495594.1:n.*1116-35T=
ENST00000286149.8:c.2344-35T= ENSP00000286149.4:n.2344-35T=
ENST00000388956.8:c.2065-35T= ENSP00000373608.4:n.2065-35T=
ENST00000388957.3:c.1330-35T= ENSP00000373609.3:n.1330-35T=
ENST00000388958.7:c.2302-35T= ENSP00000373610.3:n.2302-35T=
ENST00000563506.1:n.1361-35T=
ENST00000563871.5:n.1765-35T=
NM_001161683.1:c.2065-35T= NP_001155155.1:n.2065-35T=
NM_144672.3:c.2302-35T= NP_653273.3:n.2302-35T=
NM_170664.2:c.1330-35T= NP_733764.1:n.1330-35T=
XM_011545747.1:c.2302-35T= XP_011544049.1:n.2302-35T=
XM_011545748.1:c.1171-35T= XP_011544050.1:n.1171-35T=
NM_144672.4:c.2302-35T= MANE Select NP_653273.3:n.2302-35T=
XM_011545748.2:c.1171-35T= XP_011544050.2:n.1171-35T=
XM_017022951.1:c.568-35T= XP_016878440.1:n.568-35T=
XR_002957775.1:n.1397-35T=
NM_001161683.2:c.2065-35T= NP_001155155.1:n.2065-35T=
NM_170664.3:c.1330-35T= NP_733764.1:n.1330-35T=