Canonical Allele Identifier: CA2212563610

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710071A= , CM000678.2:g.21710071A=	GRCh38
NC_000016.9:g.21721392A= , CM000678.1:g.21721392A=	GRCh37
NC_000016.8:g.21628893A=	NCBI36
NG_012973.1:g.36558A=
NG_012973.2:g.50939A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1288A=	ENSP00000373610.3:p.Ile430=
ENST00000646100.2:c.1288A= MANE Select	ENSP00000496564.2:p.Ile430=
ENST00000647277.1:c.*102A=	ENSP00000495594.1:n.*102A=
ENST00000286149.8:c.1330A=	ENSP00000286149.4:p.Ile444=
ENST00000388956.8:c.1051A=	ENSP00000373608.4:p.Ile351=
ENST00000388957.3:c.316A=	ENSP00000373609.3:p.Ile106=
ENST00000388958.7:c.1288A=	ENSP00000373610.3:p.Ile430=
ENST00000563871.5:n.508A=
NM_001161683.1:c.1051A=	NP_001155155.1:p.Ile351=
NM_144672.3:c.1288A=	NP_653273.3:p.Ile430=
NM_170664.2:c.316A=	NP_733764.1:p.Ile106=
XM_011545747.1:c.1288A=	XP_011544049.1:p.Ile430=
XM_011545748.1:c.157A=	XP_011544050.1:p.Ile53=
NM_144672.4:c.1288A= MANE Select	NP_653273.3:p.Ile430=
XM_011545748.2:c.157A=	XP_011544050.2:p.Ile53=
XR_002957775.1:n.383A=
NM_001161683.2:c.1051A=	NP_001155155.1:p.Ile351=
NM_170664.3:c.316A=	NP_733764.1:p.Ile106=