Canonical Allele Identifier: CA2658238444
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26481003_26481008del , CM000664.2:g.26481003_26481008del GRCh38
NC_000002.11:g.26703871_26703876del , CM000664.1:g.26703871_26703876del GRCh37
NC_000002.10:g.26557375_26557380del NCBI36
NG_009937.1:g.82691_82696del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1581_1586del MANE Select ENSP00000272371.2:p.Phe528_Leu529del
ENST00000272371.6:c.1581_1586del ENSP00000272371.2:p.Phe528_Leu529del
ENST00000403946.7:c.1581_1586del ENSP00000385255.3:p.Phe528_Leu529del
NM_001287489.1:c.1581_1586del NP_001274418.1:p.Phe528_Leu529del
NM_194248.2:c.1581_1586del NP_919224.1:p.Phe528_Leu529del
XM_005264644.2:c.1626_1631del XP_005264701.1:p.Phe543_Leu544del
XM_011533185.1:c.1626_1631del XP_011531487.1:p.Phe543_Leu544del
XM_017005338.1:c.1581_1586del XP_016860827.1:p.Phe528_Leu529del
NM_001287489.2:c.1581_1586del NP_001274418.1:p.Phe528_Leu529del
NM_194248.3:c.1581_1586del MANE Select NP_919224.1:p.Phe528_Leu529del