Canonical Allele Identifier: CA2212569454

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21715016G= , CM000678.2:g.21715016G=	GRCh38
NC_000016.9:g.21726337G= , CM000678.1:g.21726337G=	GRCh37
NC_000016.8:g.21633838G=	NCBI36
NG_012973.1:g.41503G=
NG_012973.2:g.55884G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1352G=	ENSP00000373610.3:p.Gly451=
ENST00000646100.2:c.1352G= MANE Select	ENSP00000496564.2:p.Gly451=
ENST00000647277.1:c.*166G=	ENSP00000495594.1:n.*166G=
ENST00000286149.8:c.1394G=	ENSP00000286149.4:p.Gly465=
ENST00000388956.8:c.1115G=	ENSP00000373608.4:p.Gly372=
ENST00000388957.3:c.380G=	ENSP00000373609.3:p.Gly127=
ENST00000388958.7:c.1352G=	ENSP00000373610.3:p.Gly451=
ENST00000563871.5:n.572G=
NM_001161683.1:c.1115G=	NP_001155155.1:p.Gly372=
NM_144672.3:c.1352G=	NP_653273.3:p.Gly451=
NM_170664.2:c.380G=	NP_733764.1:p.Gly127=
XM_011545747.1:c.1352G=	XP_011544049.1:p.Gly451=
XM_011545748.1:c.221G=	XP_011544050.1:p.Gly74=
NM_144672.4:c.1352G= MANE Select	NP_653273.3:p.Gly451=
XM_011545748.2:c.221G=	XP_011544050.2:p.Gly74=
XR_002957775.1:n.447G=
NM_001161683.2:c.1115G=	NP_001155155.1:p.Gly372=
NM_170664.3:c.380G=	NP_733764.1:p.Gly127=