Canonical Allele Identifier: CA2212553031
Gene: OTOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21736238T= , CM000678.2:g.21736238T= GRCh38
NC_000016.9:g.21747559T= , CM000678.1:g.21747559T= GRCh37
NC_000016.8:g.21655060T= NCBI36
NG_012973.1:g.62725T=
NG_012973.2:g.77106T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000388958.8:c.2302-23T= ENSP00000373610.3:n.2302-23T=
ENST00000646100.2:c.2302-23T= MANE Select ENSP00000496564.2:n.2302-23T=
ENST00000647277.1:c.*1116-23T= ENSP00000495594.1:n.*1116-23T=
ENST00000286149.8:c.2344-23T= ENSP00000286149.4:n.2344-23T=
ENST00000388956.8:c.2065-23T= ENSP00000373608.4:n.2065-23T=
ENST00000388957.3:c.1330-23T= ENSP00000373609.3:n.1330-23T=
ENST00000388958.7:c.2302-23T= ENSP00000373610.3:n.2302-23T=
ENST00000563506.1:n.1361-23T=
ENST00000563871.5:n.1765-23T=
NM_001161683.1:c.2065-23T= NP_001155155.1:n.2065-23T=
NM_144672.3:c.2302-23T= NP_653273.3:n.2302-23T=
NM_170664.2:c.1330-23T= NP_733764.1:n.1330-23T=
XM_011545747.1:c.2302-23T= XP_011544049.1:n.2302-23T=
XM_011545748.1:c.1171-23T= XP_011544050.1:n.1171-23T=
NM_144672.4:c.2302-23T= MANE Select NP_653273.3:n.2302-23T=
XM_011545748.2:c.1171-23T= XP_011544050.2:n.1171-23T=
XM_017022951.1:c.568-23T= XP_016878440.1:n.568-23T=
XR_002957775.1:n.1397-23T=
NM_001161683.2:c.2065-23T= NP_001155155.1:n.2065-23T=
NM_170664.3:c.1330-23T= NP_733764.1:n.1330-23T=