Canonical Allele Identifier: CA395062388

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21721306A>G (hg19) ; chr16:g.21709985A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21709985A>G , CM000678.2:g.21709985A>G	GRCh38
NC_000016.9:g.21721306A>G , CM000678.1:g.21721306A>G	GRCh37
NC_000016.8:g.21628807A>G	NCBI36
NG_012973.1:g.36472A>G
NG_012973.2:g.50853A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1202A>G	ENSP00000373610.3:p.Gln401Arg
ENST00000646100.2:c.1202A>G MANE Select	ENSP00000496564.2:p.Gln401Arg
ENST00000647277.1:c.*16A>G	ENSP00000495594.1:n.*16A>G
ENST00000286149.8:c.1244A>G	ENSP00000286149.4:p.Gln415Arg
ENST00000388956.8:c.965A>G	ENSP00000373608.4:p.Gln322Arg
ENST00000388957.3:c.230A>G	ENSP00000373609.3:p.Gln77Arg
ENST00000388958.7:c.1202A>G	ENSP00000373610.3:p.Gln401Arg
ENST00000563871.5:n.422A>G
NM_001161683.1:c.965A>G	NP_001155155.1:p.Gln322Arg
NM_144672.3:c.1202A>G	NP_653273.3:p.Gln401Arg
NM_170664.2:c.230A>G	NP_733764.1:p.Gln77Arg
XM_011545747.1:c.1202A>G	XP_011544049.1:p.Gln401Arg
XM_011545748.1:c.71A>G	XP_011544050.1:p.Gln24Arg
NM_144672.4:c.1202A>G MANE Select	NP_653273.3:p.Gln401Arg
XM_011545748.2:c.71A>G	XP_011544050.2:p.Gln24Arg
XR_002957775.1:n.297A>G
NM_001161683.2:c.965A>G	NP_001155155.1:p.Gln322Arg
NM_170664.3:c.230A>G	NP_733764.1:p.Gln77Arg