Canonical Allele Identifier: CA494117562

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21721328G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710007G>A , CM000678.2:g.21710007G>A	GRCh38
NC_000016.9:g.21721328G>A , CM000678.1:g.21721328G>A	GRCh37
NC_000016.8:g.21628829G>A	NCBI36
NG_012973.1:g.36494G>A
NG_012973.2:g.50875G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1224G>A	ENSP00000373610.3:p.Glu408=
ENST00000646100.2:c.1224G>A MANE Select	ENSP00000496564.2:p.Glu408=
ENST00000647277.1:c.*38G>A	ENSP00000495594.1:n.*38G>A
ENST00000286149.8:c.1266G>A	ENSP00000286149.4:p.Glu422=
ENST00000388956.8:c.987G>A	ENSP00000373608.4:p.Glu329=
ENST00000388957.3:c.252G>A	ENSP00000373609.3:p.Glu84=
ENST00000388958.7:c.1224G>A	ENSP00000373610.3:p.Glu408=
ENST00000563871.5:n.444G>A
NM_001161683.1:c.987G>A	NP_001155155.1:p.Glu329=
NM_144672.3:c.1224G>A	NP_653273.3:p.Glu408=
NM_170664.2:c.252G>A	NP_733764.1:p.Glu84=
XM_011545747.1:c.1224G>A	XP_011544049.1:p.Glu408=
XM_011545748.1:c.93G>A	XP_011544050.1:p.Glu31=
NM_144672.4:c.1224G>A MANE Select	NP_653273.3:p.Glu408=
XM_011545748.2:c.93G>A	XP_011544050.2:p.Glu31=
XR_002957775.1:n.319G>A
NM_001161683.2:c.987G>A	NP_001155155.1:p.Glu329=
NM_170664.3:c.252G>A	NP_733764.1:p.Glu84=