Canonical Allele Identifier: CA2212563473

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21709994C= , CM000678.2:g.21709994C=	GRCh38
NC_000016.9:g.21721315C= , CM000678.1:g.21721315C=	GRCh37
NC_000016.8:g.21628816C=	NCBI36
NG_012973.1:g.36481C=
NG_012973.2:g.50862C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1211C=	ENSP00000373610.3:p.Ser404=
ENST00000646100.2:c.1211C= MANE Select	ENSP00000496564.2:p.Ser404=
ENST00000647277.1:c.*25C=	ENSP00000495594.1:n.*25C=
ENST00000286149.8:c.1253C=	ENSP00000286149.4:p.Ser418=
ENST00000388956.8:c.974C=	ENSP00000373608.4:p.Ser325=
ENST00000388957.3:c.239C=	ENSP00000373609.3:p.Ser80=
ENST00000388958.7:c.1211C=	ENSP00000373610.3:p.Ser404=
ENST00000563871.5:n.431C=
NM_001161683.1:c.974C=	NP_001155155.1:p.Ser325=
NM_144672.3:c.1211C=	NP_653273.3:p.Ser404=
NM_170664.2:c.239C=	NP_733764.1:p.Ser80=
XM_011545747.1:c.1211C=	XP_011544049.1:p.Ser404=
XM_011545748.1:c.80C=	XP_011544050.1:p.Ser27=
NM_144672.4:c.1211C= MANE Select	NP_653273.3:p.Ser404=
XM_011545748.2:c.80C=	XP_011544050.2:p.Ser27=
XR_002957775.1:n.306C=
NM_001161683.2:c.974C=	NP_001155155.1:p.Ser325=
NM_170664.3:c.239C=	NP_733764.1:p.Ser80=