Canonical Allele Identifier: CA2049208509
Gene: OTOGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358742G= , CM000674.2:g.80358742G= GRCh38
NC_000012.11:g.80752522G= , CM000674.1:g.80752522G= GRCh37
NC_000012.10:g.79276653G= NCBI36
NG_033008.1:g.154290G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6193G= MANE Select ENSP00000447211.2:p.Val2065=
ENST00000642294.1:c.133G= ENSP00000493572.1:p.Val45=
ENST00000646859.1:c.6058G= ENSP00000496036.1:p.Val2020=
ENST00000298820.7:c.1494G=
ENST00000458043.6:c.6166G= ENSP00000400895.2:p.Val2056=
ENST00000546620.5:n.449G=
ENST00000547103.5:c.6130G= ENSP00000447211.1:p.Val2044=
ENST00000550182.2:c.217G= ENSP00000449641.1:p.Val73=
ENST00000551340.5:c.321G=
NM_173591.3:c.6166G= NP_775862.3:p.Val2056=
XM_005268802.2:c.6217G= XP_005268859.1:p.Val2073=
XM_011538191.1:c.6217G= XP_011536493.1:p.Val2073=
XM_011538192.1:c.6064G= XP_011536494.1:p.Val2022=
XM_011538193.1:c.5851G= XP_011536495.1:p.Val1951=
XM_005268802.3:c.6217G= XP_005268859.1:p.Val2073=
XM_011538192.2:c.6064G= XP_011536494.1:p.Val2022=
NM_001368062.1:c.6031G= NP_001354991.1:p.Val2011=
NM_001368062.3:c.6058G= NP_001354991.2:p.Val2020=
NM_001378609.3:c.6193G= MANE Select NP_001365538.2:p.Val2065=
NM_001378610.3:c.6193G= NP_001365539.2:p.Val2065=
NM_173591.7:c.6193G= NP_775862.4:p.Val2065=