Canonical Allele Identifier: CA395062271

Gene: OTOA

Linked Data

• gnomAD v4: 16-21709960-G-A
• MyVariant Identifiers: chr16:g.21721281G>A (hg19) ; chr16:g.21709960G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21709960G>A , CM000678.2:g.21709960G>A	GRCh38
NC_000016.9:g.21721281G>A , CM000678.1:g.21721281G>A	GRCh37
NC_000016.8:g.21628782G>A	NCBI36
NG_012973.1:g.36447G>A
NG_012973.2:g.50828G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1177G>A	ENSP00000373610.3:p.Ala393Thr
ENST00000646100.2:c.1177G>A MANE Select	ENSP00000496564.2:p.Ala393Thr
ENST00000647277.1:c.1053G>A	ENSP00000495594.1:p.Met351Ile
ENST00000286149.8:c.1219G>A	ENSP00000286149.4:p.Ala407Thr
ENST00000388956.8:c.940G>A	ENSP00000373608.4:p.Ala314Thr
ENST00000388957.3:c.205G>A	ENSP00000373609.3:p.Ala69Thr
ENST00000388958.7:c.1177G>A	ENSP00000373610.3:p.Ala393Thr
ENST00000563871.5:n.397G>A
NM_001161683.1:c.940G>A	NP_001155155.1:p.Ala314Thr
NM_144672.3:c.1177G>A	NP_653273.3:p.Ala393Thr
NM_170664.2:c.205G>A	NP_733764.1:p.Ala69Thr
XM_011545747.1:c.1177G>A	XP_011544049.1:p.Ala393Thr
XM_011545748.1:c.46G>A	XP_011544050.1:p.Ala16Thr
NM_144672.4:c.1177G>A MANE Select	NP_653273.3:p.Ala393Thr
XM_011545748.2:c.46G>A	XP_011544050.2:p.Ala16Thr
XR_002957775.1:n.272G>A
NM_001161683.2:c.940G>A	NP_001155155.1:p.Ala314Thr
NM_170664.3:c.205G>A	NP_733764.1:p.Ala69Thr