Canonical Allele Identifier: CA2212553004
Gene: OTOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21736219G= , CM000678.2:g.21736219G= GRCh38
NC_000016.9:g.21747540G= , CM000678.1:g.21747540G= GRCh37
NC_000016.8:g.21655041G= NCBI36
NG_012973.1:g.62706G=
NG_012973.2:g.77087G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000388958.8:c.2302-42G= ENSP00000373610.3:n.2302-42G=
ENST00000646100.2:c.2302-42G= MANE Select ENSP00000496564.2:n.2302-42G=
ENST00000647277.1:c.*1116-42G= ENSP00000495594.1:n.*1116-42G=
ENST00000286149.8:c.2344-42G= ENSP00000286149.4:n.2344-42G=
ENST00000388956.8:c.2065-42G= ENSP00000373608.4:n.2065-42G=
ENST00000388957.3:c.1330-42G= ENSP00000373609.3:n.1330-42G=
ENST00000388958.7:c.2302-42G= ENSP00000373610.3:n.2302-42G=
ENST00000563506.1:n.1361-42G=
ENST00000563871.5:n.1765-42G=
NM_001161683.1:c.2065-42G= NP_001155155.1:n.2065-42G=
NM_144672.3:c.2302-42G= NP_653273.3:n.2302-42G=
NM_170664.2:c.1330-42G= NP_733764.1:n.1330-42G=
XM_011545747.1:c.2302-42G= XP_011544049.1:n.2302-42G=
XM_011545748.1:c.1171-42G= XP_011544050.1:n.1171-42G=
NM_144672.4:c.2302-42G= MANE Select NP_653273.3:n.2302-42G=
XM_011545748.2:c.1171-42G= XP_011544050.2:n.1171-42G=
XM_017022951.1:c.568-42G= XP_016878440.1:n.568-42G=
XR_002957775.1:n.1397-42G=
NM_001161683.2:c.2065-42G= NP_001155155.1:n.2065-42G=
NM_170664.3:c.1330-42G= NP_733764.1:n.1330-42G=