Canonical Allele Identifier: CA2529730093
Gene: OTOGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358845del , CM000674.2:g.80358845del GRCh38
NC_000012.11:g.80752625del , CM000674.1:g.80752625del GRCh37
NC_000012.10:g.79276756del NCBI36
NG_033008.1:g.154393del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6227-15del MANE Select ENSP00000447211.2:n.6227-15del
ENST00000642294.1:c.167-15del ENSP00000493572.1:n.167-15del
ENST00000646859.1:c.6092-15del ENSP00000496036.1:n.6092-15del
ENST00000298820.7:c.1527+70del
ENST00000458043.6:c.6200-15del ENSP00000400895.2:n.6200-15del
ENST00000546620.5:n.483-15del
ENST00000547103.5:c.6164-15del ENSP00000447211.1:n.6164-15del
ENST00000550182.2:c.251-15del ENSP00000449641.1:n.251-15del
ENST00000551340.5:c.355-15del
NM_173591.3:c.6200-15del NP_775862.3:n.6200-15del
XM_005268802.2:c.6251-15del XP_005268859.1:n.6251-15del
XM_011538191.1:c.6251-15del XP_011536493.1:n.6251-15del
XM_011538192.1:c.6098-15del XP_011536494.1:n.6098-15del
XM_011538193.1:c.5885-15del XP_011536495.1:n.5885-15del
XM_005268802.3:c.6251-15del XP_005268859.1:n.6251-15del
XM_011538192.2:c.6098-15del XP_011536494.1:n.6098-15del
NM_001368062.1:c.6065-15del NP_001354991.1:n.6065-15del
NM_001368062.3:c.6092-15del NP_001354991.2:n.6092-15del
NM_001378609.3:c.6227-15del MANE Select NP_001365538.2:n.6227-15del
NM_001378610.3:c.6227-15del NP_001365539.2:n.6227-15del
NM_173591.7:c.6227-15del NP_775862.4:n.6227-15del