Canonical Allele Identifier: CA2658235262
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26470491_26470493del , CM000664.2:g.26470491_26470493del GRCh38
NC_000002.11:g.26693359_26693361del , CM000664.1:g.26693359_26693361del GRCh37
NC_000002.10:g.26546863_26546865del NCBI36
NG_009937.1:g.93206_93208del

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.4023+100_4023+102del MANE Select ENSP00000272371.2:n.4023+100_4023+102del
ENST00000339598.8:c.1722+100_1722+102del MANE Plus Clinical ENSP00000344521.3:n.1722+100_1722+102del
ENST00000402415.8:c.1782+100_1782+102del ENSP00000383906.4:n.1782+100_1782+102del
ENST00000272371.6:c.4023+100_4023+102del ENSP00000272371.2:n.4023+100_4023+102del
ENST00000338581.10:c.1722+100_1722+102del ENSP00000345137.6:n.1722+100_1722+102del
ENST00000339598.7:c.1722+100_1722+102del ENSP00000344521.3:n.1722+100_1722+102del
ENST00000402415.7:c.1953+100_1953+102del ENSP00000383906.3:n.1953+100_1953+102del
ENST00000403946.7:c.4023+100_4023+102del ENSP00000385255.3:n.4023+100_4023+102del
NM_001287489.1:c.4023+100_4023+102del NP_001274418.1:n.4023+100_4023+102del
NM_004802.3:c.1722+100_1722+102del NP_004793.2:n.1722+100_1722+102del
NM_194248.2:c.4023+100_4023+102del NP_919224.1:n.4023+100_4023+102del
NM_194322.2:c.1953+100_1953+102del NP_919303.1:n.1953+100_1953+102del
NM_194323.2:c.1722+100_1722+102del NP_919304.1:n.1722+100_1722+102del
XM_005264644.2:c.4008+100_4008+102del XP_005264701.1:n.4008+100_4008+102del
XM_011533185.1:c.4068+100_4068+102del XP_011531487.1:n.4068+100_4068+102del
XM_017005338.1:c.3963+100_3963+102del XP_016860827.1:n.3963+100_3963+102del
NM_001287489.2:c.4023+100_4023+102del NP_001274418.1:n.4023+100_4023+102del
NM_004802.4:c.1722+100_1722+102del NP_004793.2:n.1722+100_1722+102del
NM_194248.3:c.4023+100_4023+102del MANE Select NP_919224.1:n.4023+100_4023+102del
NM_194322.3:c.1953+100_1953+102del NP_919303.1:n.1953+100_1953+102del
NM_194323.3:c.1722+100_1722+102del MANE Plus Clinical NP_919304.1:n.1722+100_1722+102del