Canonical Allele Identifier: CA494117570

Gene: OTOA

Linked Data

• dbSNP Id: rs1273992445
• MyVariant Identifiers: chr16:g.21721340A>G (hg19) ; chr16:g.21710019A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710019A>G , CM000678.2:g.21710019A>G	GRCh38
NC_000016.9:g.21721340A>G , CM000678.1:g.21721340A>G	GRCh37
NC_000016.8:g.21628841A>G	NCBI36
NG_012973.1:g.36506A>G
NG_012973.2:g.50887A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1236A>G	ENSP00000373610.3:p.Gly412=
ENST00000646100.2:c.1236A>G MANE Select	ENSP00000496564.2:p.Gly412=
ENST00000647277.1:c.*50A>G	ENSP00000495594.1:n.*50A>G
ENST00000286149.8:c.1278A>G	ENSP00000286149.4:p.Gly426=
ENST00000388956.8:c.999A>G	ENSP00000373608.4:p.Gly333=
ENST00000388957.3:c.264A>G	ENSP00000373609.3:p.Gly88=
ENST00000388958.7:c.1236A>G	ENSP00000373610.3:p.Gly412=
ENST00000563871.5:n.456A>G
NM_001161683.1:c.999A>G	NP_001155155.1:p.Gly333=
NM_144672.3:c.1236A>G	NP_653273.3:p.Gly412=
NM_170664.2:c.264A>G	NP_733764.1:p.Gly88=
XM_011545747.1:c.1236A>G	XP_011544049.1:p.Gly412=
XM_011545748.1:c.105A>G	XP_011544050.1:p.Gly35=
NM_144672.4:c.1236A>G MANE Select	NP_653273.3:p.Gly412=
XM_011545748.2:c.105A>G	XP_011544050.2:p.Gly35=
XR_002957775.1:n.331A>G
NM_001161683.2:c.999A>G	NP_001155155.1:p.Gly333=
NM_170664.3:c.264A>G	NP_733764.1:p.Gly88=