Canonical Allele Identifier: CA2212557618

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21705149T= , CM000678.2:g.21705149T=	GRCh38
NC_000016.9:g.21716470T= , CM000678.1:g.21716470T=	GRCh37
NC_000016.8:g.21623971T=	NCBI36
NG_012973.1:g.31636T=
NG_012973.2:g.46017T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000388958.8:c.981-20T=	ENSP00000373610.3:n.981-20T=
ENST00000646100.2:c.981-20T= MANE Select	ENSP00000496564.2:n.981-20T=
ENST00000647277.1:c.980+4122T=	ENSP00000495594.1:n.980+4122T=
ENST00000286149.8:c.1023-20T=	ENSP00000286149.4:n.1023-20T=
ENST00000388956.8:c.744-20T=	ENSP00000373608.4:n.744-20T=
ENST00000388957.3:c.9-20T=	ENSP00000373609.3:n.9-20T=
ENST00000388958.7:c.981-20T=	ENSP00000373610.3:n.981-20T=
ENST00000563871.5:n.181T=
ENST00000569064.1:n.183T=
NM_001161683.1:c.744-20T=	NP_001155155.1:n.744-20T=
NM_144672.3:c.981-20T=	NP_653273.3:n.981-20T=
NM_170664.2:c.9-20T=	NP_733764.1:n.9-20T=
XM_011545747.1:c.981-20T=	XP_011544049.1:n.981-20T=
XM_011545748.1:c.-323T=	XP_011544050.1:n.-323T=
NM_144672.4:c.981-20T= MANE Select	NP_653273.3:n.981-20T=
XM_011545748.2:c.-323T=	XP_011544050.2:n.-323T=
XR_002957775.1:n.76-20T=
NM_001161683.2:c.744-20T=	NP_001155155.1:n.744-20T=
NM_170664.3:c.9-20T=	NP_733764.1:n.9-20T=