Canonical Allele Identifier: CA2632221119
Gene: OTOA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.21722984_21722988del , CM000678.2:g.21722984_21722988del GRCh38
NC_000016.9:g.21734305_21734309del , CM000678.1:g.21734305_21734309del GRCh37
NC_000016.8:g.21641806_21641810del NCBI36
NG_012973.1:g.49471_49475del
NG_012973.2:g.63852_63856del

Transcript Alleles

HGVS Amino-acid change
ENST00000388958.8:c.1880+6_1880+10del ENSP00000373610.3:n.1880+6_1880+10del
ENST00000646100.2:c.1880+6_1880+10del MANE Select ENSP00000496564.2:n.1880+6_1880+10del
ENST00000647277.1:c.*694+6_*694+10del ENSP00000495594.1:n.*694+6_*694+10del
ENST00000286149.8:c.1922+6_1922+10del ENSP00000286149.4:n.1922+6_1922+10del
ENST00000388956.8:c.1643+6_1643+10del ENSP00000373608.4:n.1643+6_1643+10del
ENST00000388957.3:c.908+6_908+10del ENSP00000373609.3:n.908+6_908+10del
ENST00000388958.7:c.1880+6_1880+10del ENSP00000373610.3:n.1880+6_1880+10del
ENST00000563871.5:n.1295+6_1295+10del
NM_001161683.1:c.1643+6_1643+10del NP_001155155.1:n.1643+6_1643+10del
NM_144672.3:c.1880+6_1880+10del NP_653273.3:n.1880+6_1880+10del
NM_170664.2:c.908+6_908+10del NP_733764.1:n.908+6_908+10del
XM_011545747.1:c.1880+6_1880+10del XP_011544049.1:n.1880+6_1880+10del
XM_011545748.1:c.749+6_749+10del XP_011544050.1:n.749+6_749+10del
NM_144672.4:c.1880+6_1880+10del MANE Select NP_653273.3:n.1880+6_1880+10del
XM_011545748.2:c.749+6_749+10del XP_011544050.2:n.749+6_749+10del
XM_017022951.1:c.146+6_146+10del XP_016878440.1:n.146+6_146+10del
XR_002957775.1:n.975+6_975+10del
NM_001161683.2:c.1643+6_1643+10del NP_001155155.1:n.1643+6_1643+10del
NM_170664.3:c.908+6_908+10del NP_733764.1:n.908+6_908+10del