Canonical Allele Identifier: CA2049208501

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358720T= , CM000674.2:g.80358720T=	GRCh38
NC_000012.11:g.80752500T= , CM000674.1:g.80752500T=	GRCh37
NC_000012.10:g.79276631T=	NCBI36
NG_033008.1:g.154268T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6171T= MANE Select	ENSP00000447211.2:p.Asp2057=
ENST00000642294.1:c.111T=	ENSP00000493572.1:p.Asp37=
ENST00000646859.1:c.6036T=	ENSP00000496036.1:p.Asp2012=
ENST00000298820.7:c.1472T=
ENST00000458043.6:c.6144T=	ENSP00000400895.2:p.Asp2048=
ENST00000546620.5:n.427T=
ENST00000547103.5:c.6108T=	ENSP00000447211.1:p.Asp2036=
ENST00000550182.2:c.195T=	ENSP00000449641.1:p.Asp65=
ENST00000551340.5:c.299T=
NM_173591.3:c.6144T=	NP_775862.3:p.Asp2048=
XM_005268802.2:c.6195T=	XP_005268859.1:p.Asp2065=
XM_011538191.1:c.6195T=	XP_011536493.1:p.Asp2065=
XM_011538192.1:c.6042T=	XP_011536494.1:p.Asp2014=
XM_011538193.1:c.5829T=	XP_011536495.1:p.Asp1943=
XM_005268802.3:c.6195T=	XP_005268859.1:p.Asp2065=
XM_011538192.2:c.6042T=	XP_011536494.1:p.Asp2014=
NM_001368062.1:c.6009T=	NP_001354991.1:p.Asp2003=
NM_001368062.3:c.6036T=	NP_001354991.2:p.Asp2012=
NM_001378609.3:c.6171T= MANE Select	NP_001365538.2:p.Asp2057=
NM_001378610.3:c.6171T=	NP_001365539.2:p.Asp2057=
NM_173591.7:c.6171T=	NP_775862.4:p.Asp2057=