Canonical Allele Identifier: CA1028610783
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482828_26482829insATGT , CM000664.2:g.26482828_26482829insATGT GRCh38
NC_000002.11:g.26705696_26705697insATGT , CM000664.1:g.26705696_26705697insATGT GRCh37
NC_000002.10:g.26559200_26559201insATGT NCBI36
NG_009937.1:g.80870_80871insACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-237_1393-236insACAT MANE Select ENSP00000272371.2:n.1393-237_1393-236insACAT
ENST00000272371.6:c.1393-237_1393-236insACAT ENSP00000272371.2:n.1393-237_1393-236insACAT
ENST00000403946.7:c.1393-237_1393-236insACAT ENSP00000385255.3:n.1393-237_1393-236insACAT
NM_001287489.1:c.1393-237_1393-236insACAT NP_001274418.1:n.1393-237_1393-236insACAT
NM_194248.2:c.1393-237_1393-236insACAT NP_919224.1:n.1393-237_1393-236insACAT
XM_005264644.2:c.1438-237_1438-236insACAT XP_005264701.1:n.1438-237_1438-236insACAT
XM_011533185.1:c.1438-237_1438-236insACAT XP_011531487.1:n.1438-237_1438-236insACAT
XM_017005338.1:c.1393-237_1393-236insACAT XP_016860827.1:n.1393-237_1393-236insACAT
NM_001287489.2:c.1393-237_1393-236insACAT NP_001274418.1:n.1393-237_1393-236insACAT
NM_194248.3:c.1393-237_1393-236insACAT MANE Select NP_919224.1:n.1393-237_1393-236insACAT