Canonical Allele Identifier: CA395062434

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21739704A>T (hg19) ; chr16:g.21728383A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21728383A>T , CM000678.2:g.21728383A>T	GRCh38
NC_000016.9:g.21739704A>T , CM000678.1:g.21739704A>T	GRCh37
NC_000016.8:g.21647205A>T	NCBI36
NG_012973.1:g.54870A>T
NG_012973.2:g.69251A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000388958.8:c.2159A>T	ENSP00000373610.3:p.Asn720Ile
ENST00000646100.2:c.2159A>T MANE Select	ENSP00000496564.2:p.Asn720Ile
ENST00000647277.1:c.*973A>T	ENSP00000495594.1:n.*973A>T
ENST00000286149.8:c.2201A>T	ENSP00000286149.4:p.Asn734Ile
ENST00000388956.8:c.1922A>T	ENSP00000373608.4:p.Asn641Ile
ENST00000388957.3:c.1187A>T	ENSP00000373609.3:p.Asn396Ile
ENST00000388958.7:c.2159A>T	ENSP00000373610.3:p.Asn720Ile
ENST00000563871.5:n.1622A>T
NM_001161683.1:c.1922A>T	NP_001155155.1:p.Asn641Ile
NM_144672.3:c.2159A>T	NP_653273.3:p.Asn720Ile
NM_170664.2:c.1187A>T	NP_733764.1:p.Asn396Ile
XM_011545747.1:c.2159A>T	XP_011544049.1:p.Asn720Ile
XM_011545748.1:c.1028A>T	XP_011544050.1:p.Asn343Ile
NM_144672.4:c.2159A>T MANE Select	NP_653273.3:p.Asn720Ile
XM_011545748.2:c.1028A>T	XP_011544050.2:p.Asn343Ile
XM_017022951.1:c.425A>T	XP_016878440.1:p.Asn142Ile
XR_002957775.1:n.1254A>T
NM_001161683.2:c.1922A>T	NP_001155155.1:p.Asn641Ile
NM_170664.3:c.1187A>T	NP_733764.1:p.Asn396Ile