Canonical Allele Identifier: CA395062253

Gene: OTOA

Linked Data

• gnomAD v4: 16-21709957-G-A
• MyVariant Identifiers: chr16:g.21721278G>A (hg19) ; chr16:g.21709957G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21709957G>A , CM000678.2:g.21709957G>A	GRCh38
NC_000016.9:g.21721278G>A , CM000678.1:g.21721278G>A	GRCh37
NC_000016.8:g.21628779G>A	NCBI36
NG_012973.1:g.36444G>A
NG_012973.2:g.50825G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1174G>A	ENSP00000373610.3:p.Asp392Asn
ENST00000646100.2:c.1174G>A MANE Select	ENSP00000496564.2:p.Asp392Asn
ENST00000647277.1:c.1050G>A	ENSP00000495594.1:p.Arg350=
ENST00000286149.8:c.1216G>A	ENSP00000286149.4:p.Asp406Asn
ENST00000388956.8:c.937G>A	ENSP00000373608.4:p.Asp313Asn
ENST00000388957.3:c.202G>A	ENSP00000373609.3:p.Asp68Asn
ENST00000388958.7:c.1174G>A	ENSP00000373610.3:p.Asp392Asn
ENST00000563871.5:n.394G>A
NM_001161683.1:c.937G>A	NP_001155155.1:p.Asp313Asn
NM_144672.3:c.1174G>A	NP_653273.3:p.Asp392Asn
NM_170664.2:c.202G>A	NP_733764.1:p.Asp68Asn
XM_011545747.1:c.1174G>A	XP_011544049.1:p.Asp392Asn
XM_011545748.1:c.43G>A	XP_011544050.1:p.Asp15Asn
NM_144672.4:c.1174G>A MANE Select	NP_653273.3:p.Asp392Asn
XM_011545748.2:c.43G>A	XP_011544050.2:p.Asp15Asn
XR_002957775.1:n.269G>A
NM_001161683.2:c.937G>A	NP_001155155.1:p.Asp313Asn
NM_170664.3:c.202G>A	NP_733764.1:p.Asp68Asn