Canonical Allele Identifier: CA2575939972

Gene: OTOA

Linked Data

• gnomAD v4: 16-21709859-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21709859A>G , CM000678.2:g.21709859A>G	GRCh38
NC_000016.9:g.21721180A>G , CM000678.1:g.21721180A>G	GRCh37
NC_000016.8:g.21628681A>G	NCBI36
NG_012973.1:g.36346A>G
NG_012973.2:g.50727A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1105-29A>G	ENSP00000373610.3:n.1105-29A>G
ENST00000646100.2:c.1105-29A>G MANE Select	ENSP00000496564.2:n.1105-29A>G
ENST00000647277.1:c.981-29A>G	ENSP00000495594.1:n.981-29A>G
ENST00000286149.8:c.1147-29A>G	ENSP00000286149.4:n.1147-29A>G
ENST00000388956.8:c.868-29A>G	ENSP00000373608.4:n.868-29A>G
ENST00000388957.3:c.133-29A>G	ENSP00000373609.3:n.133-29A>G
ENST00000388958.7:c.1105-29A>G	ENSP00000373610.3:n.1105-29A>G
ENST00000563871.5:n.325-29A>G
ENST00000569064.1:n.479-29A>G
NM_001161683.1:c.868-29A>G	NP_001155155.1:n.868-29A>G
NM_144672.3:c.1105-29A>G	NP_653273.3:n.1105-29A>G
NM_170664.2:c.133-29A>G	NP_733764.1:n.133-29A>G
XM_011545747.1:c.1105-29A>G	XP_011544049.1:n.1105-29A>G
XM_011545748.1:c.-27-29A>G	XP_011544050.1:n.-27-29A>G
NM_144672.4:c.1105-29A>G MANE Select	NP_653273.3:n.1105-29A>G
XM_011545748.2:c.-27-29A>G	XP_011544050.2:n.-27-29A>G
XR_002957775.1:n.200-29A>G
NM_001161683.2:c.868-29A>G	NP_001155155.1:n.868-29A>G
NM_170664.3:c.133-29A>G	NP_733764.1:n.133-29A>G