Canonical Allele Identifier: CA2212563524

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710017G= , CM000678.2:g.21710017G=	GRCh38
NC_000016.9:g.21721338G= , CM000678.1:g.21721338G=	GRCh37
NC_000016.8:g.21628839G=	NCBI36
NG_012973.1:g.36504G=
NG_012973.2:g.50885G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1234G=	ENSP00000373610.3:p.Gly412=
ENST00000646100.2:c.1234G= MANE Select	ENSP00000496564.2:p.Gly412=
ENST00000647277.1:c.*48G=	ENSP00000495594.1:n.*48G=
ENST00000286149.8:c.1276G=	ENSP00000286149.4:p.Gly426=
ENST00000388956.8:c.997G=	ENSP00000373608.4:p.Gly333=
ENST00000388957.3:c.262G=	ENSP00000373609.3:p.Gly88=
ENST00000388958.7:c.1234G=	ENSP00000373610.3:p.Gly412=
ENST00000563871.5:n.454G=
NM_001161683.1:c.997G=	NP_001155155.1:p.Gly333=
NM_144672.3:c.1234G=	NP_653273.3:p.Gly412=
NM_170664.2:c.262G=	NP_733764.1:p.Gly88=
XM_011545747.1:c.1234G=	XP_011544049.1:p.Gly412=
XM_011545748.1:c.103G=	XP_011544050.1:p.Gly35=
NM_144672.4:c.1234G= MANE Select	NP_653273.3:p.Gly412=
XM_011545748.2:c.103G=	XP_011544050.2:p.Gly35=
XR_002957775.1:n.329G=
NM_001161683.2:c.997G=	NP_001155155.1:p.Gly333=
NM_170664.3:c.262G=	NP_733764.1:p.Gly88=