Canonical Allele Identifier: CA2049208493

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358699A= , CM000674.2:g.80358699A=	GRCh38
NC_000012.11:g.80752479A= , CM000674.1:g.80752479A=	GRCh37
NC_000012.10:g.79276610A=	NCBI36
NG_033008.1:g.154247A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6150A= MANE Select	ENSP00000447211.2:p.Pro2050=
ENST00000642294.1:c.90A=	ENSP00000493572.1:p.Pro30=
ENST00000646859.1:c.6015A=	ENSP00000496036.1:p.Pro2005=
ENST00000298820.7:c.1451A=
ENST00000458043.6:c.6123A=	ENSP00000400895.2:p.Pro2041=
ENST00000546620.5:n.406A=
ENST00000547103.5:c.6087A=	ENSP00000447211.1:p.Pro2029=
ENST00000550182.2:c.174A=	ENSP00000449641.1:p.Pro58=
ENST00000551340.5:c.278A=
NM_173591.3:c.6123A=	NP_775862.3:p.Pro2041=
XM_005268802.2:c.6174A=	XP_005268859.1:p.Pro2058=
XM_011538191.1:c.6174A=	XP_011536493.1:p.Pro2058=
XM_011538192.1:c.6021A=	XP_011536494.1:p.Pro2007=
XM_011538193.1:c.5808A=	XP_011536495.1:p.Pro1936=
XM_005268802.3:c.6174A=	XP_005268859.1:p.Pro2058=
XM_011538192.2:c.6021A=	XP_011536494.1:p.Pro2007=
NM_001368062.1:c.5988A=	NP_001354991.1:p.Pro1996=
NM_001368062.3:c.6015A=	NP_001354991.2:p.Pro2005=
NM_001378609.3:c.6150A= MANE Select	NP_001365538.2:p.Pro2050=
NM_001378610.3:c.6150A=	NP_001365539.2:p.Pro2050=
NM_173591.7:c.6150A=	NP_775862.4:p.Pro2050=