Canonical Allele Identifier: CA494117530

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21721283A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21709962A>G , CM000678.2:g.21709962A>G	GRCh38
NC_000016.9:g.21721283A>G , CM000678.1:g.21721283A>G	GRCh37
NC_000016.8:g.21628784A>G	NCBI36
NG_012973.1:g.36449A>G
NG_012973.2:g.50830A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1179A>G	ENSP00000373610.3:p.Ala393=
ENST00000646100.2:c.1179A>G MANE Select	ENSP00000496564.2:p.Ala393=
ENST00000647277.1:c.1055A>G	ENSP00000495594.1:p.Gln352Arg
ENST00000286149.8:c.1221A>G	ENSP00000286149.4:p.Ala407=
ENST00000388956.8:c.942A>G	ENSP00000373608.4:p.Ala314=
ENST00000388957.3:c.207A>G	ENSP00000373609.3:p.Ala69=
ENST00000388958.7:c.1179A>G	ENSP00000373610.3:p.Ala393=
ENST00000563871.5:n.399A>G
NM_001161683.1:c.942A>G	NP_001155155.1:p.Ala314=
NM_144672.3:c.1179A>G	NP_653273.3:p.Ala393=
NM_170664.2:c.207A>G	NP_733764.1:p.Ala69=
XM_011545747.1:c.1179A>G	XP_011544049.1:p.Ala393=
XM_011545748.1:c.48A>G	XP_011544050.1:p.Ala16=
NM_144672.4:c.1179A>G MANE Select	NP_653273.3:p.Ala393=
XM_011545748.2:c.48A>G	XP_011544050.2:p.Ala16=
XR_002957775.1:n.274A>G
NM_001161683.2:c.942A>G	NP_001155155.1:p.Ala314=
NM_170664.3:c.207A>G	NP_733764.1:p.Ala69=