Canonical Allele Identifier: CA2049208500

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358714A= , CM000674.2:g.80358714A=	GRCh38
NC_000012.11:g.80752494A= , CM000674.1:g.80752494A=	GRCh37
NC_000012.10:g.79276625A=	NCBI36
NG_033008.1:g.154262A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6165A= MANE Select	ENSP00000447211.2:p.Ala2055=
ENST00000642294.1:c.105A=	ENSP00000493572.1:p.Ala35=
ENST00000646859.1:c.6030A=	ENSP00000496036.1:p.Ala2010=
ENST00000298820.7:c.1466A=
ENST00000458043.6:c.6138A=	ENSP00000400895.2:p.Ala2046=
ENST00000546620.5:n.421A=
ENST00000547103.5:c.6102A=	ENSP00000447211.1:p.Ala2034=
ENST00000550182.2:c.189A=	ENSP00000449641.1:p.Ala63=
ENST00000551340.5:c.293A=
NM_173591.3:c.6138A=	NP_775862.3:p.Ala2046=
XM_005268802.2:c.6189A=	XP_005268859.1:p.Ala2063=
XM_011538191.1:c.6189A=	XP_011536493.1:p.Ala2063=
XM_011538192.1:c.6036A=	XP_011536494.1:p.Ala2012=
XM_011538193.1:c.5823A=	XP_011536495.1:p.Ala1941=
XM_005268802.3:c.6189A=	XP_005268859.1:p.Ala2063=
XM_011538192.2:c.6036A=	XP_011536494.1:p.Ala2012=
NM_001368062.1:c.6003A=	NP_001354991.1:p.Ala2001=
NM_001368062.3:c.6030A=	NP_001354991.2:p.Ala2010=
NM_001378609.3:c.6165A= MANE Select	NP_001365538.2:p.Ala2055=
NM_001378610.3:c.6165A=	NP_001365539.2:p.Ala2055=
NM_173591.7:c.6165A=	NP_775862.4:p.Ala2055=