Canonical Allele Identifier: CA395062533

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21721337C>G (hg19) ; chr16:g.21710016C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710016C>G , CM000678.2:g.21710016C>G	GRCh38
NC_000016.9:g.21721337C>G , CM000678.1:g.21721337C>G	GRCh37
NC_000016.8:g.21628838C>G	NCBI36
NG_012973.1:g.36503C>G
NG_012973.2:g.50884C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1233C>G	ENSP00000373610.3:p.His411Gln
ENST00000646100.2:c.1233C>G MANE Select	ENSP00000496564.2:p.His411Gln
ENST00000647277.1:c.*47C>G	ENSP00000495594.1:n.*47C>G
ENST00000286149.8:c.1275C>G	ENSP00000286149.4:p.His425Gln
ENST00000388956.8:c.996C>G	ENSP00000373608.4:p.His332Gln
ENST00000388957.3:c.261C>G	ENSP00000373609.3:p.His87Gln
ENST00000388958.7:c.1233C>G	ENSP00000373610.3:p.His411Gln
ENST00000563871.5:n.453C>G
NM_001161683.1:c.996C>G	NP_001155155.1:p.His332Gln
NM_144672.3:c.1233C>G	NP_653273.3:p.His411Gln
NM_170664.2:c.261C>G	NP_733764.1:p.His87Gln
XM_011545747.1:c.1233C>G	XP_011544049.1:p.His411Gln
XM_011545748.1:c.102C>G	XP_011544050.1:p.His34Gln
NM_144672.4:c.1233C>G MANE Select	NP_653273.3:p.His411Gln
XM_011545748.2:c.102C>G	XP_011544050.2:p.His34Gln
XR_002957775.1:n.328C>G
NM_001161683.2:c.996C>G	NP_001155155.1:p.His332Gln
NM_170664.3:c.261C>G	NP_733764.1:p.His87Gln