Canonical Allele Identifier: CA6701911
Gene: OTOGL HGNC NCBI

Linked Data

dbSNP Id: rs751099861

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358341A>G , CM000674.2:g.80358341A>G GRCh38
NC_000012.11:g.80752121A>G , CM000674.1:g.80752121A>G GRCh37
NC_000012.10:g.79276252A>G NCBI36
NG_033008.1:g.153889A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6113A>G MANE Select ENSP00000447211.2:p.Tyr2038Cys
ENST00000642294.1:c.53A>G ENSP00000493572.1:p.Tyr18Cys
ENST00000646859.1:c.5978A>G ENSP00000496036.1:p.Tyr1993Cys
ENST00000298820.7:c.1414A>G
ENST00000458043.6:c.6086A>G ENSP00000400895.2:p.Tyr2029Cys
ENST00000546620.5:n.369A>G
ENST00000547103.5:c.6050A>G ENSP00000447211.1:p.Tyr2017Cys
ENST00000550182.2:c.137A>G ENSP00000449641.1:p.Tyr46Cys
ENST00000551340.5:c.241A>G
NM_173591.3:c.6086A>G NP_775862.3:p.Tyr2029Cys
XM_005268802.2:c.6137A>G XP_005268859.1:p.Tyr2046Cys
XM_011538191.1:c.6137A>G XP_011536493.1:p.Tyr2046Cys
XM_011538192.1:c.5984A>G XP_011536494.1:p.Tyr1995Cys
XM_011538193.1:c.5771A>G XP_011536495.1:p.Tyr1924Cys
XM_005268802.3:c.6137A>G XP_005268859.1:p.Tyr2046Cys
XM_011538192.2:c.5984A>G XP_011536494.1:p.Tyr1995Cys
NM_001368062.1:c.5951A>G NP_001354991.1:p.Tyr1984Cys
NM_001368062.3:c.5978A>G NP_001354991.2:p.Tyr1993Cys
NM_001378609.3:c.6113A>G MANE Select NP_001365538.2:p.Tyr2038Cys
NM_001378610.3:c.6113A>G NP_001365539.2:p.Tyr2038Cys
NM_173591.7:c.6113A>G NP_775862.4:p.Tyr2038Cys