Canonical Allele Identifier: CA2658238864
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482627_26482628del , CM000664.2:g.26482627_26482628del GRCh38
NC_000002.11:g.26705495_26705496del , CM000664.1:g.26705495_26705496del GRCh37
NC_000002.10:g.26558999_26559000del NCBI36
NG_009937.1:g.81071_81072del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-36_1393-35del MANE Select ENSP00000272371.2:n.1393-36_1393-35del
ENST00000272371.6:c.1393-36_1393-35del ENSP00000272371.2:n.1393-36_1393-35del
ENST00000403946.7:c.1393-36_1393-35del ENSP00000385255.3:n.1393-36_1393-35del
NM_001287489.1:c.1393-36_1393-35del NP_001274418.1:n.1393-36_1393-35del
NM_194248.2:c.1393-36_1393-35del NP_919224.1:n.1393-36_1393-35del
XM_005264644.2:c.1438-36_1438-35del XP_005264701.1:n.1438-36_1438-35del
XM_011533185.1:c.1438-36_1438-35del XP_011531487.1:n.1438-36_1438-35del
XM_017005338.1:c.1393-36_1393-35del XP_016860827.1:n.1393-36_1393-35del
NM_001287489.2:c.1393-36_1393-35del NP_001274418.1:n.1393-36_1393-35del
NM_194248.3:c.1393-36_1393-35del MANE Select NP_919224.1:n.1393-36_1393-35del