Canonical Allele Identifier: CA2530929450
Gene: OTOGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358889_80358890del , CM000674.2:g.80358889_80358890del GRCh38
NC_000012.11:g.80752669_80752670del , CM000674.1:g.80752669_80752670del GRCh37
NC_000012.10:g.79276800_79276801del NCBI36
NG_033008.1:g.154437_154438del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6256_6257del MANE Select ENSP00000447211.2:p.Thr2086LeufsTer2
ENST00000642294.1:c.196_197del ENSP00000493572.1:p.Thr66LeufsTer2
ENST00000646859.1:c.6121_6122del ENSP00000496036.1:p.Thr2041LeufsTer2
ENST00000298820.7:c.1527+114_1527+115del
ENST00000458043.6:c.6229_6230del ENSP00000400895.2:p.Thr2077LeufsTer2
ENST00000546620.5:n.512_513del
ENST00000547103.5:c.6193_6194del ENSP00000447211.1:p.Thr2065LeufsTer2
ENST00000550182.2:c.280_281del ENSP00000449641.1:p.Thr94LeufsTer2
ENST00000551340.5:c.384_385del
NM_173591.3:c.6229_6230del NP_775862.3:p.Thr2077LeufsTer2
XM_005268802.2:c.6280_6281del XP_005268859.1:p.Thr2094LeufsTer2
XM_011538191.1:c.6280_6281del XP_011536493.1:p.Thr2094LeufsTer2
XM_011538192.1:c.6127_6128del XP_011536494.1:p.Thr2043LeufsTer2
XM_011538193.1:c.5914_5915del XP_011536495.1:p.Thr1972LeufsTer2
XM_005268802.3:c.6280_6281del XP_005268859.1:p.Thr2094LeufsTer2
XM_011538192.2:c.6127_6128del XP_011536494.1:p.Thr2043LeufsTer2
NM_001368062.1:c.6094_6095del NP_001354991.1:p.Thr2032LeufsTer2
NM_001368062.3:c.6121_6122del NP_001354991.2:p.Thr2041LeufsTer2
NM_001378609.3:c.6256_6257del MANE Select NP_001365538.2:p.Thr2086LeufsTer2
NM_001378610.3:c.6256_6257del NP_001365539.2:p.Thr2086LeufsTer2
NM_173591.7:c.6256_6257del NP_775862.4:p.Thr2086LeufsTer2