Canonical Allele Identifier: CA395062771

Gene: OTOA

Linked Data

• dbSNP Id: rs1898311697
• MyVariant Identifiers: chr16:g.21721423A>T (hg19) ; chr16:g.21710102A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710102A>T , CM000678.2:g.21710102A>T	GRCh38
NC_000016.9:g.21721423A>T , CM000678.1:g.21721423A>T	GRCh37
NC_000016.8:g.21628924A>T	NCBI36
NG_012973.1:g.36589A>T
NG_012973.2:g.50970A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1319A>T	ENSP00000373610.3:p.Lys440Met
ENST00000646100.2:c.1319A>T MANE Select	ENSP00000496564.2:p.Lys440Met
ENST00000647277.1:c.*133A>T	ENSP00000495594.1:n.*133A>T
ENST00000286149.8:c.1361A>T	ENSP00000286149.4:p.Lys454Met
ENST00000388956.8:c.1082A>T	ENSP00000373608.4:p.Lys361Met
ENST00000388957.3:c.347A>T	ENSP00000373609.3:p.Lys116Met
ENST00000388958.7:c.1319A>T	ENSP00000373610.3:p.Lys440Met
ENST00000563871.5:n.539A>T
NM_001161683.1:c.1082A>T	NP_001155155.1:p.Lys361Met
NM_144672.3:c.1319A>T	NP_653273.3:p.Lys440Met
NM_170664.2:c.347A>T	NP_733764.1:p.Lys116Met
XM_011545747.1:c.1319A>T	XP_011544049.1:p.Lys440Met
XM_011545748.1:c.188A>T	XP_011544050.1:p.Lys63Met
NM_144672.4:c.1319A>T MANE Select	NP_653273.3:p.Lys440Met
XM_011545748.2:c.188A>T	XP_011544050.2:p.Lys63Met
XR_002957775.1:n.414A>T
NM_001161683.2:c.1082A>T	NP_001155155.1:p.Lys361Met
NM_170664.3:c.347A>T	NP_733764.1:p.Lys116Met