Canonical Allele Identifier: CA2573134383
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26479603dup , CM000664.2:g.26479603dup GRCh38
NC_000002.11:g.26702471dup , CM000664.1:g.26702471dup GRCh37
NC_000002.10:g.26555975dup NCBI36
NG_009937.1:g.84099dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1966dup MANE Select ENSP00000272371.2:p.Arg656ProfsTer7
ENST00000272371.6:c.1966dup ENSP00000272371.2:p.Arg656ProfsTer7
ENST00000403946.7:c.1966dup ENSP00000385255.3:p.Arg656ProfsTer7
NM_001287489.1:c.1966dup NP_001274418.1:p.Arg656ProfsTer7
NM_194248.2:c.1966dup NP_919224.1:p.Arg656ProfsTer7
XM_005264644.2:c.2011dup XP_005264701.1:p.Arg671ProfsTer7
XM_011533185.1:c.2011dup XP_011531487.1:p.Arg671ProfsTer7
XM_017005338.1:c.1966dup XP_016860827.1:p.Arg656ProfsTer7
NM_001287489.2:c.1966dup NP_001274418.1:p.Arg656ProfsTer7
NM_194248.3:c.1966dup MANE Select NP_919224.1:p.Arg656ProfsTer7