Canonical Allele Identifier: CA2212574804
Gene: OTOA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21722998C= , CM000678.2:g.21722998C= GRCh38
NC_000016.9:g.21734319C= , CM000678.1:g.21734319C= GRCh37
NC_000016.8:g.21641820C= NCBI36
NG_012973.1:g.49485C=
NG_012973.2:g.63866C=

Transcript Alleles

HGVS Amino-acid change
ENST00000388958.8:c.1880+20C= ENSP00000373610.3:n.1880+20C=
ENST00000646100.2:c.1880+20C= MANE Select ENSP00000496564.2:n.1880+20C=
ENST00000647277.1:c.*694+20C= ENSP00000495594.1:n.*694+20C=
ENST00000286149.8:c.1922+20C= ENSP00000286149.4:n.1922+20C=
ENST00000388956.8:c.1643+20C= ENSP00000373608.4:n.1643+20C=
ENST00000388957.3:c.908+20C= ENSP00000373609.3:n.908+20C=
ENST00000388958.7:c.1880+20C= ENSP00000373610.3:n.1880+20C=
ENST00000563871.5:n.1295+20C=
NM_001161683.1:c.1643+20C= NP_001155155.1:n.1643+20C=
NM_144672.3:c.1880+20C= NP_653273.3:n.1880+20C=
NM_170664.2:c.908+20C= NP_733764.1:n.908+20C=
XM_011545747.1:c.1880+20C= XP_011544049.1:n.1880+20C=
XM_011545748.1:c.749+20C= XP_011544050.1:n.749+20C=
NM_144672.4:c.1880+20C= MANE Select NP_653273.3:n.1880+20C=
XM_011545748.2:c.749+20C= XP_011544050.2:n.749+20C=
XM_017022951.1:c.146+20C= XP_016878440.1:n.146+20C=
XR_002957775.1:n.975+20C=
NM_001161683.2:c.1643+20C= NP_001155155.1:n.1643+20C=
NM_170664.3:c.908+20C= NP_733764.1:n.908+20C=