Canonical Allele Identifier: CA2212574793

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21722978C= , CM000678.2:g.21722978C=	GRCh38
NC_000016.9:g.21734299C= , CM000678.1:g.21734299C=	GRCh37
NC_000016.8:g.21641800C=	NCBI36
NG_012973.1:g.49465C=
NG_012973.2:g.63846C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1880C=	ENSP00000373610.3:p.Pro627=
ENST00000646100.2:c.1880C= MANE Select	ENSP00000496564.2:p.Pro627=
ENST00000647277.1:c.*694C=	ENSP00000495594.1:n.*694C=
ENST00000286149.8:c.1922C=	ENSP00000286149.4:p.Pro641=
ENST00000388956.8:c.1643C=	ENSP00000373608.4:p.Pro548=
ENST00000388957.3:c.908C=	ENSP00000373609.3:p.Pro303=
ENST00000388958.7:c.1880C=	ENSP00000373610.3:p.Pro627=
ENST00000563871.5:n.1295C=
NM_001161683.1:c.1643C=	NP_001155155.1:p.Pro548=
NM_144672.3:c.1880C=	NP_653273.3:p.Pro627=
NM_170664.2:c.908C=	NP_733764.1:p.Pro303=
XM_011545747.1:c.1880C=	XP_011544049.1:p.Pro627=
XM_011545748.1:c.749C=	XP_011544050.1:p.Pro250=
NM_144672.4:c.1880C= MANE Select	NP_653273.3:p.Pro627=
XM_011545748.2:c.749C=	XP_011544050.2:p.Pro250=
XM_017022951.1:c.146C=	XP_016878440.1:p.Pro49=
XR_002957775.1:n.975C=
NM_001161683.2:c.1643C=	NP_001155155.1:p.Pro548=
NM_170664.3:c.908C=	NP_733764.1:p.Pro303=