Canonical Allele Identifier: CA2049208494

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358702A= , CM000674.2:g.80358702A=	GRCh38
NC_000012.11:g.80752482A= , CM000674.1:g.80752482A=	GRCh37
NC_000012.10:g.79276613A=	NCBI36
NG_033008.1:g.154250A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6153A= MANE Select	ENSP00000447211.2:p.Leu2051=
ENST00000642294.1:c.93A=	ENSP00000493572.1:p.Leu31=
ENST00000646859.1:c.6018A=	ENSP00000496036.1:p.Leu2006=
ENST00000298820.7:c.1454A=
ENST00000458043.6:c.6126A=	ENSP00000400895.2:p.Leu2042=
ENST00000546620.5:n.409A=
ENST00000547103.5:c.6090A=	ENSP00000447211.1:p.Leu2030=
ENST00000550182.2:c.177A=	ENSP00000449641.1:p.Leu59=
ENST00000551340.5:c.281A=
NM_173591.3:c.6126A=	NP_775862.3:p.Leu2042=
XM_005268802.2:c.6177A=	XP_005268859.1:p.Leu2059=
XM_011538191.1:c.6177A=	XP_011536493.1:p.Leu2059=
XM_011538192.1:c.6024A=	XP_011536494.1:p.Leu2008=
XM_011538193.1:c.5811A=	XP_011536495.1:p.Leu1937=
XM_005268802.3:c.6177A=	XP_005268859.1:p.Leu2059=
XM_011538192.2:c.6024A=	XP_011536494.1:p.Leu2008=
NM_001368062.1:c.5991A=	NP_001354991.1:p.Leu1997=
NM_001368062.3:c.6018A=	NP_001354991.2:p.Leu2006=
NM_001378609.3:c.6153A= MANE Select	NP_001365538.2:p.Leu2051=
NM_001378610.3:c.6153A=	NP_001365539.2:p.Leu2051=
NM_173591.7:c.6153A=	NP_775862.4:p.Leu2051=