Canonical Allele Identifier: CA2749241678
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26519342del , CM000664.2:g.26519342del GRCh38
NC_000002.11:g.26742210del , CM000664.1:g.26742210del GRCh37
NC_000002.10:g.26595714del NCBI36
NG_009937.1:g.44360del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.228-230del MANE Select ENSP00000272371.2:n.228-230del
ENST00000272371.6:c.228-230del ENSP00000272371.2:n.228-230del
ENST00000403946.7:c.228-230del ENSP00000385255.3:n.228-230del
NM_001287489.1:c.228-230del NP_001274418.1:n.228-230del
NM_194248.2:c.228-230del NP_919224.1:n.228-230del
XM_005264644.2:c.228-230del XP_005264701.1:n.228-230del
XM_011533185.1:c.228-230del XP_011531487.1:n.228-230del
XM_017005338.1:c.228-230del XP_016860827.1:n.228-230del
NM_001287489.2:c.228-230del NP_001274418.1:n.228-230del
NM_194248.3:c.228-230del MANE Select NP_919224.1:n.228-230del