Canonical Allele Identifier: CA2575940198

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21736250_21736252del , CM000678.2:g.21736250_21736252del	GRCh38
NC_000016.9:g.21747571_21747573del , CM000678.1:g.21747571_21747573del	GRCh37
NC_000016.8:g.21655072_21655074del	NCBI36
NG_012973.1:g.62737_62739del
NG_012973.2:g.77118_77120del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.2302-11_2302-9del	ENSP00000373610.3:n.2302-11_2302-9del
ENST00000646100.2:c.2302-11_2302-9del MANE Select	ENSP00000496564.2:n.2302-11_2302-9del
ENST00000647277.1:c.*1116-11_*1116-9del	ENSP00000495594.1:n.*1116-11_*1116-9del
ENST00000286149.8:c.2344-11_2344-9del	ENSP00000286149.4:n.2344-11_2344-9del
ENST00000388956.8:c.2065-11_2065-9del	ENSP00000373608.4:n.2065-11_2065-9del
ENST00000388957.3:c.1330-11_1330-9del	ENSP00000373609.3:n.1330-11_1330-9del
ENST00000388958.7:c.2302-11_2302-9del	ENSP00000373610.3:n.2302-11_2302-9del
ENST00000563506.1:n.1361-11_1361-9del
ENST00000563871.5:n.1765-11_1765-9del
NM_001161683.1:c.2065-11_2065-9del	NP_001155155.1:n.2065-11_2065-9del
NM_144672.3:c.2302-11_2302-9del	NP_653273.3:n.2302-11_2302-9del
NM_170664.2:c.1330-11_1330-9del	NP_733764.1:n.1330-11_1330-9del
XM_011545747.1:c.2302-11_2302-9del	XP_011544049.1:n.2302-11_2302-9del
XM_011545748.1:c.1171-11_1171-9del	XP_011544050.1:n.1171-11_1171-9del
NM_144672.4:c.2302-11_2302-9del MANE Select	NP_653273.3:n.2302-11_2302-9del
XM_011545748.2:c.1171-11_1171-9del	XP_011544050.2:n.1171-11_1171-9del
XM_017022951.1:c.568-11_568-9del	XP_016878440.1:n.568-11_568-9del
XR_002957775.1:n.1397-11_1397-9del
NM_001161683.2:c.2065-11_2065-9del	NP_001155155.1:n.2065-11_2065-9del
NM_170664.3:c.1330-11_1330-9del	NP_733764.1:n.1330-11_1330-9del