Canonical Allele Identifier: CA395062518

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21721335C>A (hg19) ; chr16:g.21710014C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710014C>A , CM000678.2:g.21710014C>A	GRCh38
NC_000016.9:g.21721335C>A , CM000678.1:g.21721335C>A	GRCh37
NC_000016.8:g.21628836C>A	NCBI36
NG_012973.1:g.36501C>A
NG_012973.2:g.50882C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1231C>A	ENSP00000373610.3:p.His411Asn
ENST00000646100.2:c.1231C>A MANE Select	ENSP00000496564.2:p.His411Asn
ENST00000647277.1:c.*45C>A	ENSP00000495594.1:n.*45C>A
ENST00000286149.8:c.1273C>A	ENSP00000286149.4:p.His425Asn
ENST00000388956.8:c.994C>A	ENSP00000373608.4:p.His332Asn
ENST00000388957.3:c.259C>A	ENSP00000373609.3:p.His87Asn
ENST00000388958.7:c.1231C>A	ENSP00000373610.3:p.His411Asn
ENST00000563871.5:n.451C>A
NM_001161683.1:c.994C>A	NP_001155155.1:p.His332Asn
NM_144672.3:c.1231C>A	NP_653273.3:p.His411Asn
NM_170664.2:c.259C>A	NP_733764.1:p.His87Asn
XM_011545747.1:c.1231C>A	XP_011544049.1:p.His411Asn
XM_011545748.1:c.100C>A	XP_011544050.1:p.His34Asn
NM_144672.4:c.1231C>A MANE Select	NP_653273.3:p.His411Asn
XM_011545748.2:c.100C>A	XP_011544050.2:p.His34Asn
XR_002957775.1:n.326C>A
NM_001161683.2:c.994C>A	NP_001155155.1:p.His332Asn
NM_170664.3:c.259C>A	NP_733764.1:p.His87Asn