Canonical Allele Identifier: CA494117673
Gene: OTOA HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.21721424G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21710103G>A , CM000678.2:g.21710103G>A GRCh38
NC_000016.9:g.21721424G>A , CM000678.1:g.21721424G>A GRCh37
NC_000016.8:g.21628925G>A NCBI36
NG_012973.1:g.36590G>A
NG_012973.2:g.50971G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000388958.8:c.1320G>A ENSP00000373610.3:p.Lys440=
ENST00000646100.2:c.1320G>A MANE Select ENSP00000496564.2:p.Lys440=
ENST00000647277.1:c.*134G>A ENSP00000495594.1:n.*134G>A
ENST00000286149.8:c.1362G>A ENSP00000286149.4:p.Lys454=
ENST00000388956.8:c.1083G>A ENSP00000373608.4:p.Lys361=
ENST00000388957.3:c.348G>A ENSP00000373609.3:p.Lys116=
ENST00000388958.7:c.1320G>A ENSP00000373610.3:p.Lys440=
ENST00000563871.5:n.540G>A
NM_001161683.1:c.1083G>A NP_001155155.1:p.Lys361=
NM_144672.3:c.1320G>A NP_653273.3:p.Lys440=
NM_170664.2:c.348G>A NP_733764.1:p.Lys116=
XM_011545747.1:c.1320G>A XP_011544049.1:p.Lys440=
XM_011545748.1:c.189G>A XP_011544050.1:p.Lys63=
NM_144672.4:c.1320G>A MANE Select NP_653273.3:p.Lys440=
XM_011545748.2:c.189G>A XP_011544050.2:p.Lys63=
XR_002957775.1:n.415G>A
NM_001161683.2:c.1083G>A NP_001155155.1:p.Lys361=
NM_170664.3:c.348G>A NP_733764.1:p.Lys116=