Canonical Allele Identifier: CA2212553002

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21736219_21736220delinsGT , CM000678.2:g.21736219_21736220delinsGT	GRCh38
NC_000016.9:g.21747540_21747541delinsGT , CM000678.1:g.21747540_21747541delinsGT	GRCh37
NC_000016.8:g.21655041_21655042delinsGT	NCBI36
NG_012973.1:g.62706_62707delinsGT
NG_012973.2:g.77087_77088delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.2302-42_2302-41delinsGT	ENSP00000373610.3:n.2302-42_2302-41delinsGT
ENST00000646100.2:c.2302-42_2302-41delinsGT MANE Select	ENSP00000496564.2:n.2302-42_2302-41delinsGT
ENST00000647277.1:c.*1116-42_*1116-41delinsGT	ENSP00000495594.1:n.*1116-42_*1116-41delinsGT
ENST00000286149.8:c.2344-42_2344-41delinsGT	ENSP00000286149.4:n.2344-42_2344-41delinsGT
ENST00000388956.8:c.2065-42_2065-41delinsGT	ENSP00000373608.4:n.2065-42_2065-41delinsGT
ENST00000388957.3:c.1330-42_1330-41delinsGT	ENSP00000373609.3:n.1330-42_1330-41delinsGT
ENST00000388958.7:c.2302-42_2302-41delinsGT	ENSP00000373610.3:n.2302-42_2302-41delinsGT
ENST00000563506.1:n.1361-42_1361-41delinsGT
ENST00000563871.5:n.1765-42_1765-41delinsGT
NM_001161683.1:c.2065-42_2065-41delinsGT	NP_001155155.1:n.2065-42_2065-41delinsGT
NM_144672.3:c.2302-42_2302-41delinsGT	NP_653273.3:n.2302-42_2302-41delinsGT
NM_170664.2:c.1330-42_1330-41delinsGT	NP_733764.1:n.1330-42_1330-41delinsGT
XM_011545747.1:c.2302-42_2302-41delinsGT	XP_011544049.1:n.2302-42_2302-41delinsGT
XM_011545748.1:c.1171-42_1171-41delinsGT	XP_011544050.1:n.1171-42_1171-41delinsGT
NM_144672.4:c.2302-42_2302-41delinsGT MANE Select	NP_653273.3:n.2302-42_2302-41delinsGT
XM_011545748.2:c.1171-42_1171-41delinsGT	XP_011544050.2:n.1171-42_1171-41delinsGT
XM_017022951.1:c.568-42_568-41delinsGT	XP_016878440.1:n.568-42_568-41delinsGT
XR_002957775.1:n.1397-42_1397-41delinsGT
NM_001161683.2:c.2065-42_2065-41delinsGT	NP_001155155.1:n.2065-42_2065-41delinsGT
NM_170664.3:c.1330-42_1330-41delinsGT	NP_733764.1:n.1330-42_1330-41delinsGT