Canonical Allele Identifier: CA2620017016
Gene: OTOGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358536_80358541del , CM000674.2:g.80358536_80358541del GRCh38
NC_000012.11:g.80752316_80752321del , CM000674.1:g.80752316_80752321del GRCh37
NC_000012.10:g.79276447_79276452del NCBI36
NG_033008.1:g.154084_154089del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6122-135_6122-130del MANE Select ENSP00000447211.2:n.6122-135_6122-130del
ENST00000642294.1:c.62-135_62-130del ENSP00000493572.1:n.62-135_62-130del
ENST00000646859.1:c.5987-135_5987-130del ENSP00000496036.1:n.5987-135_5987-130del
ENST00000298820.7:c.1423-135_1423-130del
ENST00000458043.6:c.6095-135_6095-130del ENSP00000400895.2:n.6095-135_6095-130del
ENST00000546620.5:n.378-135_378-130del
ENST00000547103.5:c.6059-135_6059-130del ENSP00000447211.1:n.6059-135_6059-130del
ENST00000550182.2:c.146-135_146-130del ENSP00000449641.1:n.146-135_146-130del
ENST00000551340.5:c.250-135_250-130del
NM_173591.3:c.6095-135_6095-130del NP_775862.3:n.6095-135_6095-130del
XM_005268802.2:c.6146-135_6146-130del XP_005268859.1:n.6146-135_6146-130del
XM_011538191.1:c.6146-135_6146-130del XP_011536493.1:n.6146-135_6146-130del
XM_011538192.1:c.5993-135_5993-130del XP_011536494.1:n.5993-135_5993-130del
XM_011538193.1:c.5780-135_5780-130del XP_011536495.1:n.5780-135_5780-130del
XM_005268802.3:c.6146-135_6146-130del XP_005268859.1:n.6146-135_6146-130del
XM_011538192.2:c.5993-135_5993-130del XP_011536494.1:n.5993-135_5993-130del
NM_001368062.1:c.5960-135_5960-130del NP_001354991.1:n.5960-135_5960-130del
NM_001368062.3:c.5987-135_5987-130del NP_001354991.2:n.5987-135_5987-130del
NM_001378609.3:c.6122-135_6122-130del MANE Select NP_001365538.2:n.6122-135_6122-130del
NM_001378610.3:c.6122-135_6122-130del NP_001365539.2:n.6122-135_6122-130del
NM_173591.7:c.6122-135_6122-130del NP_775862.4:n.6122-135_6122-130del