Canonical Allele Identifier: CA2212553040

Gene: OTOA

Linked Data

• dbSNP Id: rs1414727179

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21736246T>G , CM000678.2:g.21736246T>G	GRCh38
NC_000016.9:g.21747567T>G , CM000678.1:g.21747567T>G	GRCh37
NC_000016.8:g.21655068T>G	NCBI36
NG_012973.1:g.62733T>G
NG_012973.2:g.77114T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.2302-15T>G	ENSP00000373610.3:n.2302-15T>G
ENST00000646100.2:c.2302-15T>G MANE Select	ENSP00000496564.2:n.2302-15T>G
ENST00000647277.1:c.*1116-15T>G	ENSP00000495594.1:n.*1116-15T>G
ENST00000286149.8:c.2344-15T>G	ENSP00000286149.4:n.2344-15T>G
ENST00000388956.8:c.2065-15T>G	ENSP00000373608.4:n.2065-15T>G
ENST00000388957.3:c.1330-15T>G	ENSP00000373609.3:n.1330-15T>G
ENST00000388958.7:c.2302-15T>G	ENSP00000373610.3:n.2302-15T>G
ENST00000563506.1:n.1361-15T>G
ENST00000563871.5:n.1765-15T>G
NM_001161683.1:c.2065-15T>G	NP_001155155.1:n.2065-15T>G
NM_144672.3:c.2302-15T>G	NP_653273.3:n.2302-15T>G
NM_170664.2:c.1330-15T>G	NP_733764.1:n.1330-15T>G
XM_011545747.1:c.2302-15T>G	XP_011544049.1:n.2302-15T>G
XM_011545748.1:c.1171-15T>G	XP_011544050.1:n.1171-15T>G
NM_144672.4:c.2302-15T>G MANE Select	NP_653273.3:n.2302-15T>G
XM_011545748.2:c.1171-15T>G	XP_011544050.2:n.1171-15T>G
XM_017022951.1:c.568-15T>G	XP_016878440.1:n.568-15T>G
XR_002957775.1:n.1397-15T>G
NM_001161683.2:c.2065-15T>G	NP_001155155.1:n.2065-15T>G
NM_170664.3:c.1330-15T>G	NP_733764.1:n.1330-15T>G