Canonical Allele Identifier: CA494117613

Gene: OTOA

Linked Data

• gnomAD v4: 16-21710058-G-A
• MyVariant Identifiers: chr16:g.21721379G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710058G>A , CM000678.2:g.21710058G>A	GRCh38
NC_000016.9:g.21721379G>A , CM000678.1:g.21721379G>A	GRCh37
NC_000016.8:g.21628880G>A	NCBI36
NG_012973.1:g.36545G>A
NG_012973.2:g.50926G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1275G>A	ENSP00000373610.3:p.Lys425=
ENST00000646100.2:c.1275G>A MANE Select	ENSP00000496564.2:p.Lys425=
ENST00000647277.1:c.*89G>A	ENSP00000495594.1:n.*89G>A
ENST00000286149.8:c.1317G>A	ENSP00000286149.4:p.Lys439=
ENST00000388956.8:c.1038G>A	ENSP00000373608.4:p.Lys346=
ENST00000388957.3:c.303G>A	ENSP00000373609.3:p.Lys101=
ENST00000388958.7:c.1275G>A	ENSP00000373610.3:p.Lys425=
ENST00000563871.5:n.495G>A
NM_001161683.1:c.1038G>A	NP_001155155.1:p.Lys346=
NM_144672.3:c.1275G>A	NP_653273.3:p.Lys425=
NM_170664.2:c.303G>A	NP_733764.1:p.Lys101=
XM_011545747.1:c.1275G>A	XP_011544049.1:p.Lys425=
XM_011545748.1:c.144G>A	XP_011544050.1:p.Lys48=
NM_144672.4:c.1275G>A MANE Select	NP_653273.3:p.Lys425=
XM_011545748.2:c.144G>A	XP_011544050.2:p.Lys48=
XR_002957775.1:n.370G>A
NM_001161683.2:c.1038G>A	NP_001155155.1:p.Lys346=
NM_170664.3:c.303G>A	NP_733764.1:p.Lys101=