Canonical Allele Identifier: CA2658239500
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26483670_26483684del , CM000664.2:g.26483670_26483684del GRCh38
NC_000002.11:g.26706538_26706552del , CM000664.1:g.26706538_26706552del GRCh37
NC_000002.10:g.26560042_26560056del NCBI36
NG_009937.1:g.80020_80034del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1206-31_1206-17del MANE Select ENSP00000272371.2:n.1206-31_1206-17del
ENST00000272371.6:c.1206-31_1206-17del ENSP00000272371.2:n.1206-31_1206-17del
ENST00000403946.7:c.1206-31_1206-17del ENSP00000385255.3:n.1206-31_1206-17del
NM_001287489.1:c.1206-31_1206-17del NP_001274418.1:n.1206-31_1206-17del
NM_194248.2:c.1206-31_1206-17del NP_919224.1:n.1206-31_1206-17del
XM_005264644.2:c.1251-31_1251-17del XP_005264701.1:n.1251-31_1251-17del
XM_011533185.1:c.1251-31_1251-17del XP_011531487.1:n.1251-31_1251-17del
XM_017005338.1:c.1206-31_1206-17del XP_016860827.1:n.1206-31_1206-17del
NM_001287489.2:c.1206-31_1206-17del NP_001274418.1:n.1206-31_1206-17del
NM_194248.3:c.1206-31_1206-17del MANE Select NP_919224.1:n.1206-31_1206-17del