Canonical Allele Identifier: CA2212563619

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710082C= , CM000678.2:g.21710082C=	GRCh38
NC_000016.9:g.21721403C= , CM000678.1:g.21721403C=	GRCh37
NC_000016.8:g.21628904C=	NCBI36
NG_012973.1:g.36569C=
NG_012973.2:g.50950C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1299C=	ENSP00000373610.3:p.Ala433=
ENST00000646100.2:c.1299C= MANE Select	ENSP00000496564.2:p.Ala433=
ENST00000647277.1:c.*113C=	ENSP00000495594.1:n.*113C=
ENST00000286149.8:c.1341C=	ENSP00000286149.4:p.Ala447=
ENST00000388956.8:c.1062C=	ENSP00000373608.4:p.Ala354=
ENST00000388957.3:c.327C=	ENSP00000373609.3:p.Ala109=
ENST00000388958.7:c.1299C=	ENSP00000373610.3:p.Ala433=
ENST00000563871.5:n.519C=
NM_001161683.1:c.1062C=	NP_001155155.1:p.Ala354=
NM_144672.3:c.1299C=	NP_653273.3:p.Ala433=
NM_170664.2:c.327C=	NP_733764.1:p.Ala109=
XM_011545747.1:c.1299C=	XP_011544049.1:p.Ala433=
XM_011545748.1:c.168C=	XP_011544050.1:p.Ala56=
NM_144672.4:c.1299C= MANE Select	NP_653273.3:p.Ala433=
XM_011545748.2:c.168C=	XP_011544050.2:p.Ala56=
XR_002957775.1:n.394C=
NM_001161683.2:c.1062C=	NP_001155155.1:p.Ala354=
NM_170664.3:c.327C=	NP_733764.1:p.Ala109=