Canonical Allele Identifier: CA2212563573

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710039A= , CM000678.2:g.21710039A=	GRCh38
NC_000016.9:g.21721360A= , CM000678.1:g.21721360A=	GRCh37
NC_000016.8:g.21628861A=	NCBI36
NG_012973.1:g.36526A=
NG_012973.2:g.50907A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1256A=	ENSP00000373610.3:p.Gln419=
ENST00000646100.2:c.1256A= MANE Select	ENSP00000496564.2:p.Gln419=
ENST00000647277.1:c.*70A=	ENSP00000495594.1:n.*70A=
ENST00000286149.8:c.1298A=	ENSP00000286149.4:p.Gln433=
ENST00000388956.8:c.1019A=	ENSP00000373608.4:p.Gln340=
ENST00000388957.3:c.284A=	ENSP00000373609.3:p.Gln95=
ENST00000388958.7:c.1256A=	ENSP00000373610.3:p.Gln419=
ENST00000563871.5:n.476A=
NM_001161683.1:c.1019A=	NP_001155155.1:p.Gln340=
NM_144672.3:c.1256A=	NP_653273.3:p.Gln419=
NM_170664.2:c.284A=	NP_733764.1:p.Gln95=
XM_011545747.1:c.1256A=	XP_011544049.1:p.Gln419=
XM_011545748.1:c.125A=	XP_011544050.1:p.Gln42=
NM_144672.4:c.1256A= MANE Select	NP_653273.3:p.Gln419=
XM_011545748.2:c.125A=	XP_011544050.2:p.Gln42=
XR_002957775.1:n.351A=
NM_001161683.2:c.1019A=	NP_001155155.1:p.Gln340=
NM_170664.3:c.284A=	NP_733764.1:p.Gln95=