Canonical Allele Identifier: CA494117583

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21721352C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21710031C>A , CM000678.2:g.21710031C>A	GRCh38
NC_000016.9:g.21721352C>A , CM000678.1:g.21721352C>A	GRCh37
NC_000016.8:g.21628853C>A	NCBI36
NG_012973.1:g.36518C>A
NG_012973.2:g.50899C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1248C>A	ENSP00000373610.3:p.Thr416=
ENST00000646100.2:c.1248C>A MANE Select	ENSP00000496564.2:p.Thr416=
ENST00000647277.1:c.*62C>A	ENSP00000495594.1:n.*62C>A
ENST00000286149.8:c.1290C>A	ENSP00000286149.4:p.Thr430=
ENST00000388956.8:c.1011C>A	ENSP00000373608.4:p.Thr337=
ENST00000388957.3:c.276C>A	ENSP00000373609.3:p.Thr92=
ENST00000388958.7:c.1248C>A	ENSP00000373610.3:p.Thr416=
ENST00000563871.5:n.468C>A
NM_001161683.1:c.1011C>A	NP_001155155.1:p.Thr337=
NM_144672.3:c.1248C>A	NP_653273.3:p.Thr416=
NM_170664.2:c.276C>A	NP_733764.1:p.Thr92=
XM_011545747.1:c.1248C>A	XP_011544049.1:p.Thr416=
XM_011545748.1:c.117C>A	XP_011544050.1:p.Thr39=
NM_144672.4:c.1248C>A MANE Select	NP_653273.3:p.Thr416=
XM_011545748.2:c.117C>A	XP_011544050.2:p.Thr39=
XR_002957775.1:n.343C>A
NM_001161683.2:c.1011C>A	NP_001155155.1:p.Thr337=
NM_170664.3:c.276C>A	NP_733764.1:p.Thr92=