Canonical Allele Identifier: CA2212563261
Gene: OTOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21709874_21709875delinsTG , CM000678.2:g.21709874_21709875delinsTG GRCh38
NC_000016.9:g.21721195_21721196delinsTG , CM000678.1:g.21721195_21721196delinsTG GRCh37
NC_000016.8:g.21628696_21628697delinsTG NCBI36
NG_012973.1:g.36361_36362delinsTG
NG_012973.2:g.50742_50743delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000388958.8:c.1105-14_1105-13delinsTG ENSP00000373610.3:n.1105-14_1105-13delinsTG
ENST00000646100.2:c.1105-14_1105-13delinsTG MANE Select ENSP00000496564.2:n.1105-14_1105-13delinsTG
ENST00000647277.1:c.981-14_981-13delinsTG ENSP00000495594.1:n.981-14_981-13delinsTG
ENST00000286149.8:c.1147-14_1147-13delinsTG ENSP00000286149.4:n.1147-14_1147-13delinsTG
ENST00000388956.8:c.868-14_868-13delinsTG ENSP00000373608.4:n.868-14_868-13delinsTG
ENST00000388957.3:c.133-14_133-13delinsTG ENSP00000373609.3:n.133-14_133-13delinsTG
ENST00000388958.7:c.1105-14_1105-13delinsTG ENSP00000373610.3:n.1105-14_1105-13delinsTG
ENST00000563871.5:n.325-14_325-13delinsTG
ENST00000569064.1:n.479-14_479-13delinsTG
NM_001161683.1:c.868-14_868-13delinsTG NP_001155155.1:n.868-14_868-13delinsTG
NM_144672.3:c.1105-14_1105-13delinsTG NP_653273.3:n.1105-14_1105-13delinsTG
NM_170664.2:c.133-14_133-13delinsTG NP_733764.1:n.133-14_133-13delinsTG
XM_011545747.1:c.1105-14_1105-13delinsTG XP_011544049.1:n.1105-14_1105-13delinsTG
XM_011545748.1:c.-27-14_-27-13delinsTG XP_011544050.1:n.-27-14_-27-13delinsTG
NM_144672.4:c.1105-14_1105-13delinsTG MANE Select NP_653273.3:n.1105-14_1105-13delinsTG
XM_011545748.2:c.-27-14_-27-13delinsTG XP_011544050.2:n.-27-14_-27-13delinsTG
XR_002957775.1:n.200-14_200-13delinsTG
NM_001161683.2:c.868-14_868-13delinsTG NP_001155155.1:n.868-14_868-13delinsTG
NM_170664.3:c.133-14_133-13delinsTG NP_733764.1:n.133-14_133-13delinsTG