Canonical Allele Identifier: CA395062037

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21739597C>G (hg19) ; chr16:g.21728276C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21728276C>G , CM000678.2:g.21728276C>G	GRCh38
NC_000016.9:g.21739597C>G , CM000678.1:g.21739597C>G	GRCh37
NC_000016.8:g.21647098C>G	NCBI36
NG_012973.1:g.54763C>G
NG_012973.2:g.69144C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000388958.8:c.2052C>G	ENSP00000373610.3:p.Ile684Met
ENST00000646100.2:c.2052C>G MANE Select	ENSP00000496564.2:p.Ile684Met
ENST00000647277.1:c.*866C>G	ENSP00000495594.1:n.*866C>G
ENST00000286149.8:c.2094C>G	ENSP00000286149.4:p.Ile698Met
ENST00000388956.8:c.1815C>G	ENSP00000373608.4:p.Ile605Met
ENST00000388957.3:c.1080C>G	ENSP00000373609.3:p.Ile360Met
ENST00000388958.7:c.2052C>G	ENSP00000373610.3:p.Ile684Met
ENST00000563871.5:n.1515C>G
NM_001161683.1:c.1815C>G	NP_001155155.1:p.Ile605Met
NM_144672.3:c.2052C>G	NP_653273.3:p.Ile684Met
NM_170664.2:c.1080C>G	NP_733764.1:p.Ile360Met
XM_011545747.1:c.2052C>G	XP_011544049.1:p.Ile684Met
XM_011545748.1:c.921C>G	XP_011544050.1:p.Ile307Met
NM_144672.4:c.2052C>G MANE Select	NP_653273.3:p.Ile684Met
XM_011545748.2:c.921C>G	XP_011544050.2:p.Ile307Met
XM_017022951.1:c.318C>G	XP_016878440.1:p.Ile106Met
XR_002957775.1:n.1147C>G
NM_001161683.2:c.1815C>G	NP_001155155.1:p.Ile605Met
NM_170664.3:c.1080C>G	NP_733764.1:p.Ile360Met