Canonical Allele Identifier: CA2796693842
Gene: OTOGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358350_80358356del , CM000674.2:g.80358350_80358356del GRCh38
NC_000012.11:g.80752130_80752136del , CM000674.1:g.80752130_80752136del GRCh37
NC_000012.10:g.79276261_79276267del NCBI36
NG_033008.1:g.153898_153904del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6121+1_6121+7del
ENST00000642294.1:c.61+1_61+7del
ENST00000646859.1:c.5986+1_5986+7del
ENST00000298820.7:c.1422+1_1422+7del
ENST00000458043.6:c.6094+1_6094+7del
ENST00000546620.5:n.377+1_377+7del
ENST00000547103.5:c.6058+1_6058+7del
ENST00000550182.2:c.145+1_145+7del
ENST00000551340.5:c.249+1_249+7del
NM_173591.3:c.6094+1_6094+7del
XM_005268802.2:c.6145+1_6145+7del
XM_011538191.1:c.6145+1_6145+7del
XM_011538192.1:c.5992+1_5992+7del
XM_011538193.1:c.5779+1_5779+7del
XM_005268802.3:c.6145+1_6145+7del
XM_011538192.2:c.5992+1_5992+7del
NM_001368062.1:c.5959+1_5959+7del
NM_001368062.3:c.5986+1_5986+7del
NM_001378609.3:c.6121+1_6121+7del
NM_001378610.3:c.6121+1_6121+7del
NM_173591.7:c.6121+1_6121+7del