Canonical Allele Identifier: CA531762011
Gene: OTOF HGNC NCBI

Linked Data

dbSNP Id: rs1345989143

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480955_26480956del , CM000664.2:g.26480955_26480956del GRCh38
NC_000002.11:g.26703823_26703824del , CM000664.1:g.26703823_26703824del GRCh37
NC_000002.10:g.26557327_26557328del NCBI36
NG_009937.1:g.82743_82744del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1633_1634del MANE Select ENSP00000272371.2:p.Asn545LeufsTer6
ENST00000272371.6:c.1633_1634del ENSP00000272371.2:p.Asn545LeufsTer6
ENST00000403946.7:c.1633_1634del ENSP00000385255.3:p.Asn545LeufsTer6
NM_001287489.1:c.1633_1634del NP_001274418.1:p.Asn545LeufsTer6
NM_194248.2:c.1633_1634del NP_919224.1:p.Asn545LeufsTer6
XM_005264644.2:c.1678_1679del XP_005264701.1:p.Asn560LeufsTer6
XM_011533185.1:c.1678_1679del XP_011531487.1:p.Asn560LeufsTer6
XM_017005338.1:c.1633_1634del XP_016860827.1:p.Asn545LeufsTer6
NM_001287489.2:c.1633_1634del NP_001274418.1:p.Asn545LeufsTer6
NM_194248.3:c.1633_1634del MANE Select NP_919224.1:p.Asn545LeufsTer6