Canonical Allele Identifier: CA2550146141
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482756_26482757insATGCATGT , CM000664.2:g.26482756_26482757insATGCATGT GRCh38
NC_000002.11:g.26705624_26705625insATGCATGT , CM000664.1:g.26705624_26705625insATGCATGT GRCh37
NC_000002.10:g.26559128_26559129insATGCATGT NCBI36
NG_009937.1:g.80942_80943insACATGCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-165_1393-164insACATGCAT MANE Select ENSP00000272371.2:n.1393-165_1393-164insACATGCAT
ENST00000272371.6:c.1393-165_1393-164insACATGCAT ENSP00000272371.2:n.1393-165_1393-164insACATGCAT
ENST00000403946.7:c.1393-165_1393-164insACATGCAT ENSP00000385255.3:n.1393-165_1393-164insACATGCAT
NM_001287489.1:c.1393-165_1393-164insACATGCAT NP_001274418.1:n.1393-165_1393-164insACATGCAT
NM_194248.2:c.1393-165_1393-164insACATGCAT NP_919224.1:n.1393-165_1393-164insACATGCAT
XM_005264644.2:c.1438-165_1438-164insACATGCAT XP_005264701.1:n.1438-165_1438-164insACATGCAT
XM_011533185.1:c.1438-165_1438-164insACATGCAT XP_011531487.1:n.1438-165_1438-164insACATGCAT
XM_017005338.1:c.1393-165_1393-164insACATGCAT XP_016860827.1:n.1393-165_1393-164insACATGCAT
NM_001287489.2:c.1393-165_1393-164insACATGCAT NP_001274418.1:n.1393-165_1393-164insACATGCAT
NM_194248.3:c.1393-165_1393-164insACATGCAT MANE Select NP_919224.1:n.1393-165_1393-164insACATGCAT