Canonical Allele Identifier: CA2575939974

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21709867T>G , CM000678.2:g.21709867T>G	GRCh38
NC_000016.9:g.21721188T>G , CM000678.1:g.21721188T>G	GRCh37
NC_000016.8:g.21628689T>G	NCBI36
NG_012973.1:g.36354T>G
NG_012973.2:g.50735T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000388958.8:c.1105-21T>G	ENSP00000373610.3:n.1105-21T>G
ENST00000646100.2:c.1105-21T>G MANE Select	ENSP00000496564.2:n.1105-21T>G
ENST00000647277.1:c.981-21T>G	ENSP00000495594.1:n.981-21T>G
ENST00000286149.8:c.1147-21T>G	ENSP00000286149.4:n.1147-21T>G
ENST00000388956.8:c.868-21T>G	ENSP00000373608.4:n.868-21T>G
ENST00000388957.3:c.133-21T>G	ENSP00000373609.3:n.133-21T>G
ENST00000388958.7:c.1105-21T>G	ENSP00000373610.3:n.1105-21T>G
ENST00000563871.5:n.325-21T>G
ENST00000569064.1:n.479-21T>G
NM_001161683.1:c.868-21T>G	NP_001155155.1:n.868-21T>G
NM_144672.3:c.1105-21T>G	NP_653273.3:n.1105-21T>G
NM_170664.2:c.133-21T>G	NP_733764.1:n.133-21T>G
XM_011545747.1:c.1105-21T>G	XP_011544049.1:n.1105-21T>G
XM_011545748.1:c.-27-21T>G	XP_011544050.1:n.-27-21T>G
NM_144672.4:c.1105-21T>G MANE Select	NP_653273.3:n.1105-21T>G
XM_011545748.2:c.-27-21T>G	XP_011544050.2:n.-27-21T>G
XR_002957775.1:n.200-21T>G
NM_001161683.2:c.868-21T>G	NP_001155155.1:n.868-21T>G
NM_170664.3:c.133-21T>G	NP_733764.1:n.133-21T>G