Canonical Allele Identifier: CA2212563490

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710000C= , CM000678.2:g.21710000C=	GRCh38
NC_000016.9:g.21721321C= , CM000678.1:g.21721321C=	GRCh37
NC_000016.8:g.21628822C=	NCBI36
NG_012973.1:g.36487C=
NG_012973.2:g.50868C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1217C=	ENSP00000373610.3:p.Ser406=
ENST00000646100.2:c.1217C= MANE Select	ENSP00000496564.2:p.Ser406=
ENST00000647277.1:c.*31C=	ENSP00000495594.1:n.*31C=
ENST00000286149.8:c.1259C=	ENSP00000286149.4:p.Ser420=
ENST00000388956.8:c.980C=	ENSP00000373608.4:p.Ser327=
ENST00000388957.3:c.245C=	ENSP00000373609.3:p.Ser82=
ENST00000388958.7:c.1217C=	ENSP00000373610.3:p.Ser406=
ENST00000563871.5:n.437C=
NM_001161683.1:c.980C=	NP_001155155.1:p.Ser327=
NM_144672.3:c.1217C=	NP_653273.3:p.Ser406=
NM_170664.2:c.245C=	NP_733764.1:p.Ser82=
XM_011545747.1:c.1217C=	XP_011544049.1:p.Ser406=
XM_011545748.1:c.86C=	XP_011544050.1:p.Ser29=
NM_144672.4:c.1217C= MANE Select	NP_653273.3:p.Ser406=
XM_011545748.2:c.86C=	XP_011544050.2:p.Ser29=
XR_002957775.1:n.312C=
NM_001161683.2:c.980C=	NP_001155155.1:p.Ser327=
NM_170664.3:c.245C=	NP_733764.1:p.Ser82=