Canonical Allele Identifier: CA2049208569

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358871G= , CM000674.2:g.80358871G=	GRCh38
NC_000012.11:g.80752651G= , CM000674.1:g.80752651G=	GRCh37
NC_000012.10:g.79276782G=	NCBI36
NG_033008.1:g.154419G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6238G= MANE Select	ENSP00000447211.2:p.Glu2080=
ENST00000642294.1:c.178G=	ENSP00000493572.1:p.Glu60=
ENST00000646859.1:c.6103G=	ENSP00000496036.1:p.Glu2035=
ENST00000298820.7:c.1527+96G=
ENST00000458043.6:c.6211G=	ENSP00000400895.2:p.Glu2071=
ENST00000546620.5:n.494G=
ENST00000547103.5:c.6175G=	ENSP00000447211.1:p.Glu2059=
ENST00000550182.2:c.262G=	ENSP00000449641.1:p.Glu88=
ENST00000551340.5:c.366G=
NM_173591.3:c.6211G=	NP_775862.3:p.Glu2071=
XM_005268802.2:c.6262G=	XP_005268859.1:p.Glu2088=
XM_011538191.1:c.6262G=	XP_011536493.1:p.Glu2088=
XM_011538192.1:c.6109G=	XP_011536494.1:p.Glu2037=
XM_011538193.1:c.5896G=	XP_011536495.1:p.Glu1966=
XM_005268802.3:c.6262G=	XP_005268859.1:p.Glu2088=
XM_011538192.2:c.6109G=	XP_011536494.1:p.Glu2037=
NM_001368062.1:c.6076G=	NP_001354991.1:p.Glu2026=
NM_001368062.3:c.6103G=	NP_001354991.2:p.Glu2035=
NM_001378609.3:c.6238G= MANE Select	NP_001365538.2:p.Glu2080=
NM_001378610.3:c.6238G=	NP_001365539.2:p.Glu2080=
NM_173591.7:c.6238G=	NP_775862.4:p.Glu2080=