Canonical Allele Identifier: CA2049208586
Gene: OTOGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358907_80358908delinsAC , CM000674.2:g.80358907_80358908delinsAC GRCh38
NC_000012.11:g.80752687_80752688delinsAC , CM000674.1:g.80752687_80752688delinsAC GRCh37
NC_000012.10:g.79276818_79276819delinsAC NCBI36
NG_033008.1:g.154455_154456delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6267+7_6267+8delinsAC MANE Select ENSP00000447211.2:n.6267+7_6267+8delinsAC
ENST00000642294.1:c.207+7_207+8delinsAC ENSP00000493572.1:n.207+7_207+8delinsAC
ENST00000646859.1:c.6132+7_6132+8delinsAC ENSP00000496036.1:n.6132+7_6132+8delinsAC
ENST00000298820.7:c.1527+132_1527+133delinsAC
ENST00000458043.6:c.6240+7_6240+8delinsAC ENSP00000400895.2:n.6240+7_6240+8delinsAC
ENST00000546620.5:n.523+7_523+8delinsAC
ENST00000547103.5:c.6204+7_6204+8delinsAC ENSP00000447211.1:n.6204+7_6204+8delinsAC
ENST00000550182.2:c.291+7_291+8delinsAC ENSP00000449641.1:n.291+7_291+8delinsAC
ENST00000551340.5:c.395+7_395+8delinsAC
NM_173591.3:c.6240+7_6240+8delinsAC NP_775862.3:n.6240+7_6240+8delinsAC
XM_005268802.2:c.6291+7_6291+8delinsAC XP_005268859.1:n.6291+7_6291+8delinsAC
XM_011538191.1:c.6291+7_6291+8delinsAC XP_011536493.1:n.6291+7_6291+8delinsAC
XM_011538192.1:c.6138+7_6138+8delinsAC XP_011536494.1:n.6138+7_6138+8delinsAC
XM_011538193.1:c.5925+7_5925+8delinsAC XP_011536495.1:n.5925+7_5925+8delinsAC
XM_005268802.3:c.6291+7_6291+8delinsAC XP_005268859.1:n.6291+7_6291+8delinsAC
XM_011538192.2:c.6138+7_6138+8delinsAC XP_011536494.1:n.6138+7_6138+8delinsAC
NM_001368062.1:c.6105+7_6105+8delinsAC NP_001354991.1:n.6105+7_6105+8delinsAC
NM_001368062.3:c.6132+7_6132+8delinsAC NP_001354991.2:n.6132+7_6132+8delinsAC
NM_001378609.3:c.6267+7_6267+8delinsAC MANE Select NP_001365538.2:n.6267+7_6267+8delinsAC
NM_001378610.3:c.6267+7_6267+8delinsAC NP_001365539.2:n.6267+7_6267+8delinsAC
NM_173591.7:c.6267+7_6267+8delinsAC NP_775862.4:n.6267+7_6267+8delinsAC