Canonical Allele Identifier: CA7952577
Gene: OTOA HGNC NCBI

Linked Data

dbSNP Id: rs758587527

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21710042T>C , CM000678.2:g.21710042T>C GRCh38
NC_000016.9:g.21721363T>C , CM000678.1:g.21721363T>C GRCh37
NC_000016.8:g.21628864T>C NCBI36
NG_012973.1:g.36529T>C
NG_012973.2:g.50910T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000388958.8:c.1259T>C ENSP00000373610.3:p.Val420Ala
ENST00000646100.2:c.1259T>C MANE Select ENSP00000496564.2:p.Val420Ala
ENST00000647277.1:c.*73T>C ENSP00000495594.1:n.*73T>C
ENST00000286149.8:c.1301T>C ENSP00000286149.4:p.Val434Ala
ENST00000388956.8:c.1022T>C ENSP00000373608.4:p.Val341Ala
ENST00000388957.3:c.287T>C ENSP00000373609.3:p.Val96Ala
ENST00000388958.7:c.1259T>C ENSP00000373610.3:p.Val420Ala
ENST00000563871.5:n.479T>C
NM_001161683.1:c.1022T>C NP_001155155.1:p.Val341Ala
NM_144672.3:c.1259T>C NP_653273.3:p.Val420Ala
NM_170664.2:c.287T>C NP_733764.1:p.Val96Ala
XM_011545747.1:c.1259T>C XP_011544049.1:p.Val420Ala
XM_011545748.1:c.128T>C XP_011544050.1:p.Val43Ala
NM_144672.4:c.1259T>C MANE Select NP_653273.3:p.Val420Ala
XM_011545748.2:c.128T>C XP_011544050.2:p.Val43Ala
XR_002957775.1:n.354T>C
NM_001161683.2:c.1022T>C NP_001155155.1:p.Val341Ala
NM_170664.3:c.287T>C NP_733764.1:p.Val96Ala