Canonical Allele Identifier: CA385888878
Gene: OTOGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358771C>A , CM000674.2:g.80358771C>A GRCh38
NC_000012.11:g.80752551C>A , CM000674.1:g.80752551C>A GRCh37
NC_000012.10:g.79276682C>A NCBI36
NG_033008.1:g.154319C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6222C>A MANE Select ENSP00000447211.2:p.His2074Gln
ENST00000642294.1:c.162C>A ENSP00000493572.1:p.His54Gln
ENST00000646859.1:c.6087C>A ENSP00000496036.1:p.His2029Gln
ENST00000298820.7:c.1523C>A
ENST00000458043.6:c.6195C>A ENSP00000400895.2:p.His2065Gln
ENST00000546620.5:n.478C>A
ENST00000547103.5:c.6159C>A ENSP00000447211.1:p.His2053Gln
ENST00000550182.2:c.246C>A ENSP00000449641.1:p.His82Gln
ENST00000551340.5:c.350C>A
NM_173591.3:c.6195C>A NP_775862.3:p.His2065Gln
XM_005268802.2:c.6246C>A XP_005268859.1:p.His2082Gln
XM_011538191.1:c.6246C>A XP_011536493.1:p.His2082Gln
XM_011538192.1:c.6093C>A XP_011536494.1:p.His2031Gln
XM_011538193.1:c.5880C>A XP_011536495.1:p.His1960Gln
XM_005268802.3:c.6246C>A XP_005268859.1:p.His2082Gln
XM_011538192.2:c.6093C>A XP_011536494.1:p.His2031Gln
NM_001368062.1:c.6060C>A NP_001354991.1:p.His2020Gln
NM_001368062.3:c.6087C>A NP_001354991.2:p.His2029Gln
NM_001378609.3:c.6222C>A MANE Select NP_001365538.2:p.His2074Gln
NM_001378610.3:c.6222C>A NP_001365539.2:p.His2074Gln
NM_173591.7:c.6222C>A NP_775862.4:p.His2074Gln