Canonical Allele Identifier: CA2536923081
Gene: OTOGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358597_80358598del , CM000674.2:g.80358597_80358598del GRCh38
NC_000012.11:g.80752377_80752378del , CM000674.1:g.80752377_80752378del GRCh37
NC_000012.10:g.79276508_79276509del NCBI36
NG_033008.1:g.154145_154146del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6122-74_6122-73del MANE Select ENSP00000447211.2:n.6122-74_6122-73del
ENST00000642294.1:c.62-74_62-73del ENSP00000493572.1:n.62-74_62-73del
ENST00000646859.1:c.5987-74_5987-73del ENSP00000496036.1:n.5987-74_5987-73del
ENST00000298820.7:c.1423-74_1423-73del
ENST00000458043.6:c.6095-74_6095-73del ENSP00000400895.2:n.6095-74_6095-73del
ENST00000546620.5:n.378-74_378-73del
ENST00000547103.5:c.6059-74_6059-73del ENSP00000447211.1:n.6059-74_6059-73del
ENST00000550182.2:c.146-74_146-73del ENSP00000449641.1:n.146-74_146-73del
ENST00000551340.5:c.250-74_250-73del
NM_173591.3:c.6095-74_6095-73del NP_775862.3:n.6095-74_6095-73del
XM_005268802.2:c.6146-74_6146-73del XP_005268859.1:n.6146-74_6146-73del
XM_011538191.1:c.6146-74_6146-73del XP_011536493.1:n.6146-74_6146-73del
XM_011538192.1:c.5993-74_5993-73del XP_011536494.1:n.5993-74_5993-73del
XM_011538193.1:c.5780-74_5780-73del XP_011536495.1:n.5780-74_5780-73del
XM_005268802.3:c.6146-74_6146-73del XP_005268859.1:n.6146-74_6146-73del
XM_011538192.2:c.5993-74_5993-73del XP_011536494.1:n.5993-74_5993-73del
NM_001368062.1:c.5960-74_5960-73del NP_001354991.1:n.5960-74_5960-73del
NM_001368062.3:c.5987-74_5987-73del NP_001354991.2:n.5987-74_5987-73del
NM_001378609.3:c.6122-74_6122-73del MANE Select NP_001365538.2:n.6122-74_6122-73del
NM_001378610.3:c.6122-74_6122-73del NP_001365539.2:n.6122-74_6122-73del
NM_173591.7:c.6122-74_6122-73del NP_775862.4:n.6122-74_6122-73del