Canonical Allele Identifier: CA395062582

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21721347T>G (hg19) ; chr16:g.21710026T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710026T>G , CM000678.2:g.21710026T>G	GRCh38
NC_000016.9:g.21721347T>G , CM000678.1:g.21721347T>G	GRCh37
NC_000016.8:g.21628848T>G	NCBI36
NG_012973.1:g.36513T>G
NG_012973.2:g.50894T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1243T>G	ENSP00000373610.3:p.Ser415Ala
ENST00000646100.2:c.1243T>G MANE Select	ENSP00000496564.2:p.Ser415Ala
ENST00000647277.1:c.*57T>G	ENSP00000495594.1:n.*57T>G
ENST00000286149.8:c.1285T>G	ENSP00000286149.4:p.Ser429Ala
ENST00000388956.8:c.1006T>G	ENSP00000373608.4:p.Ser336Ala
ENST00000388957.3:c.271T>G	ENSP00000373609.3:p.Ser91Ala
ENST00000388958.7:c.1243T>G	ENSP00000373610.3:p.Ser415Ala
ENST00000563871.5:n.463T>G
NM_001161683.1:c.1006T>G	NP_001155155.1:p.Ser336Ala
NM_144672.3:c.1243T>G	NP_653273.3:p.Ser415Ala
NM_170664.2:c.271T>G	NP_733764.1:p.Ser91Ala
XM_011545747.1:c.1243T>G	XP_011544049.1:p.Ser415Ala
XM_011545748.1:c.112T>G	XP_011544050.1:p.Ser38Ala
NM_144672.4:c.1243T>G MANE Select	NP_653273.3:p.Ser415Ala
XM_011545748.2:c.112T>G	XP_011544050.2:p.Ser38Ala
XR_002957775.1:n.338T>G
NM_001161683.2:c.1006T>G	NP_001155155.1:p.Ser336Ala
NM_170664.3:c.271T>G	NP_733764.1:p.Ser91Ala