Canonical Allele Identifier: CA494117605

Gene: OTOA

Linked Data

• gnomAD v4: 16-21710046-A-C
• MyVariant Identifiers: chr16:g.21721367A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710046A>C , CM000678.2:g.21710046A>C	GRCh38
NC_000016.9:g.21721367A>C , CM000678.1:g.21721367A>C	GRCh37
NC_000016.8:g.21628868A>C	NCBI36
NG_012973.1:g.36533A>C
NG_012973.2:g.50914A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1263A>C	ENSP00000373610.3:p.Ser421=
ENST00000646100.2:c.1263A>C MANE Select	ENSP00000496564.2:p.Ser421=
ENST00000647277.1:c.*77A>C	ENSP00000495594.1:n.*77A>C
ENST00000286149.8:c.1305A>C	ENSP00000286149.4:p.Ser435=
ENST00000388956.8:c.1026A>C	ENSP00000373608.4:p.Ser342=
ENST00000388957.3:c.291A>C	ENSP00000373609.3:p.Ser97=
ENST00000388958.7:c.1263A>C	ENSP00000373610.3:p.Ser421=
ENST00000563871.5:n.483A>C
NM_001161683.1:c.1026A>C	NP_001155155.1:p.Ser342=
NM_144672.3:c.1263A>C	NP_653273.3:p.Ser421=
NM_170664.2:c.291A>C	NP_733764.1:p.Ser97=
XM_011545747.1:c.1263A>C	XP_011544049.1:p.Ser421=
XM_011545748.1:c.132A>C	XP_011544050.1:p.Ser44=
NM_144672.4:c.1263A>C MANE Select	NP_653273.3:p.Ser421=
XM_011545748.2:c.132A>C	XP_011544050.2:p.Ser44=
XR_002957775.1:n.358A>C
NM_001161683.2:c.1026A>C	NP_001155155.1:p.Ser342=
NM_170664.3:c.291A>C	NP_733764.1:p.Ser97=