Canonical Allele Identifier: CA2212577114

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21728386C= , CM000678.2:g.21728386C=	GRCh38
NC_000016.9:g.21739707C= , CM000678.1:g.21739707C=	GRCh37
NC_000016.8:g.21647208C=	NCBI36
NG_012973.1:g.54873C=
NG_012973.2:g.69254C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000388958.8:c.2162C=	ENSP00000373610.3:p.Pro721=
ENST00000646100.2:c.2162C= MANE Select	ENSP00000496564.2:p.Pro721=
ENST00000647277.1:c.*976C=	ENSP00000495594.1:n.*976C=
ENST00000286149.8:c.2204C=	ENSP00000286149.4:p.Pro735=
ENST00000388956.8:c.1925C=	ENSP00000373608.4:p.Pro642=
ENST00000388957.3:c.1190C=	ENSP00000373609.3:p.Pro397=
ENST00000388958.7:c.2162C=	ENSP00000373610.3:p.Pro721=
ENST00000563871.5:n.1625C=
NM_001161683.1:c.1925C=	NP_001155155.1:p.Pro642=
NM_144672.3:c.2162C=	NP_653273.3:p.Pro721=
NM_170664.2:c.1190C=	NP_733764.1:p.Pro397=
XM_011545747.1:c.2162C=	XP_011544049.1:p.Pro721=
XM_011545748.1:c.1031C=	XP_011544050.1:p.Pro344=
NM_144672.4:c.2162C= MANE Select	NP_653273.3:p.Pro721=
XM_011545748.2:c.1031C=	XP_011544050.2:p.Pro344=
XM_017022951.1:c.428C=	XP_016878440.1:p.Pro143=
XR_002957775.1:n.1257C=
NM_001161683.2:c.1925C=	NP_001155155.1:p.Pro642=
NM_170664.3:c.1190C=	NP_733764.1:p.Pro397=