Canonical Allele Identifier: CA2212563693

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710124C= , CM000678.2:g.21710124C=	GRCh38
NC_000016.9:g.21721445C= , CM000678.1:g.21721445C=	GRCh37
NC_000016.8:g.21628946C=	NCBI36
NG_012973.1:g.36611C=
NG_012973.2:g.50992C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1320+21C=	ENSP00000373610.3:n.1320+21C=
ENST00000646100.2:c.1320+21C= MANE Select	ENSP00000496564.2:n.1320+21C=
ENST00000647277.1:c.*134+21C=	ENSP00000495594.1:n.*134+21C=
ENST00000286149.8:c.1362+21C=	ENSP00000286149.4:n.1362+21C=
ENST00000388956.8:c.1083+21C=	ENSP00000373608.4:n.1083+21C=
ENST00000388957.3:c.348+21C=	ENSP00000373609.3:n.348+21C=
ENST00000388958.7:c.1320+21C=	ENSP00000373610.3:n.1320+21C=
ENST00000563871.5:n.540+21C=
NM_001161683.1:c.1083+21C=	NP_001155155.1:n.1083+21C=
NM_144672.3:c.1320+21C=	NP_653273.3:n.1320+21C=
NM_170664.2:c.348+21C=	NP_733764.1:n.348+21C=
XM_011545747.1:c.1320+21C=	XP_011544049.1:n.1320+21C=
XM_011545748.1:c.189+21C=	XP_011544050.1:n.189+21C=
NM_144672.4:c.1320+21C= MANE Select	NP_653273.3:n.1320+21C=
XM_011545748.2:c.189+21C=	XP_011544050.2:n.189+21C=
XR_002957775.1:n.415+21C=
NM_001161683.2:c.1083+21C=	NP_001155155.1:n.1083+21C=
NM_170664.3:c.348+21C=	NP_733764.1:n.348+21C=