Canonical Allele Identifier: CA2212563601

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710061C= , CM000678.2:g.21710061C=	GRCh38
NC_000016.9:g.21721382C= , CM000678.1:g.21721382C=	GRCh37
NC_000016.8:g.21628883C=	NCBI36
NG_012973.1:g.36548C=
NG_012973.2:g.50929C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1278C=	ENSP00000373610.3:p.Ser426=
ENST00000646100.2:c.1278C= MANE Select	ENSP00000496564.2:p.Ser426=
ENST00000647277.1:c.*92C=	ENSP00000495594.1:n.*92C=
ENST00000286149.8:c.1320C=	ENSP00000286149.4:p.Ser440=
ENST00000388956.8:c.1041C=	ENSP00000373608.4:p.Ser347=
ENST00000388957.3:c.306C=	ENSP00000373609.3:p.Ser102=
ENST00000388958.7:c.1278C=	ENSP00000373610.3:p.Ser426=
ENST00000563871.5:n.498C=
NM_001161683.1:c.1041C=	NP_001155155.1:p.Ser347=
NM_144672.3:c.1278C=	NP_653273.3:p.Ser426=
NM_170664.2:c.306C=	NP_733764.1:p.Ser102=
XM_011545747.1:c.1278C=	XP_011544049.1:p.Ser426=
XM_011545748.1:c.147C=	XP_011544050.1:p.Ser49=
NM_144672.4:c.1278C= MANE Select	NP_653273.3:p.Ser426=
XM_011545748.2:c.147C=	XP_011544050.2:p.Ser49=
XR_002957775.1:n.373C=
NM_001161683.2:c.1041C=	NP_001155155.1:p.Ser347=
NM_170664.3:c.306C=	NP_733764.1:p.Ser102=