Canonical Allele Identifier: CA1028609649
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480957_26480958insAAAAA , CM000664.2:g.26480957_26480958insAAAAA GRCh38
NC_000002.11:g.26703825_26703826insAAAAA , CM000664.1:g.26703825_26703826insAAAAA GRCh37
NC_000002.10:g.26557329_26557330insAAAAA NCBI36
NG_009937.1:g.82742_82743insTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1632_1633insTTTTT MANE Select ENSP00000272371.2:p.Asn545PhefsTer13
ENST00000272371.6:c.1632_1633insTTTTT ENSP00000272371.2:p.Asn545PhefsTer13
ENST00000403946.7:c.1632_1633insTTTTT ENSP00000385255.3:p.Asn545PhefsTer13
NM_001287489.1:c.1632_1633insTTTTT NP_001274418.1:p.Asn545PhefsTer13
NM_194248.2:c.1632_1633insTTTTT NP_919224.1:p.Asn545PhefsTer13
XM_005264644.2:c.1677_1678insTTTTT XP_005264701.1:p.Asn560PhefsTer13
XM_011533185.1:c.1677_1678insTTTTT XP_011531487.1:p.Asn560PhefsTer13
XM_017005338.1:c.1632_1633insTTTTT XP_016860827.1:p.Asn545PhefsTer13
NM_001287489.2:c.1632_1633insTTTTT NP_001274418.1:p.Asn545PhefsTer13
NM_194248.3:c.1632_1633insTTTTT MANE Select NP_919224.1:p.Asn545PhefsTer13