Canonical Allele Identifier: CA2049208514

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358752A= , CM000674.2:g.80358752A=	GRCh38
NC_000012.11:g.80752532A= , CM000674.1:g.80752532A=	GRCh37
NC_000012.10:g.79276663A=	NCBI36
NG_033008.1:g.154300A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6203A= MANE Select	ENSP00000447211.2:p.Gln2068=
ENST00000642294.1:c.143A=	ENSP00000493572.1:p.Gln48=
ENST00000646859.1:c.6068A=	ENSP00000496036.1:p.Gln2023=
ENST00000298820.7:c.1504A=
ENST00000458043.6:c.6176A=	ENSP00000400895.2:p.Gln2059=
ENST00000546620.5:n.459A=
ENST00000547103.5:c.6140A=	ENSP00000447211.1:p.Gln2047=
ENST00000550182.2:c.227A=	ENSP00000449641.1:p.Gln76=
ENST00000551340.5:c.331A=
NM_173591.3:c.6176A=	NP_775862.3:p.Gln2059=
XM_005268802.2:c.6227A=	XP_005268859.1:p.Gln2076=
XM_011538191.1:c.6227A=	XP_011536493.1:p.Gln2076=
XM_011538192.1:c.6074A=	XP_011536494.1:p.Gln2025=
XM_011538193.1:c.5861A=	XP_011536495.1:p.Gln1954=
XM_005268802.3:c.6227A=	XP_005268859.1:p.Gln2076=
XM_011538192.2:c.6074A=	XP_011536494.1:p.Gln2025=
NM_001368062.1:c.6041A=	NP_001354991.1:p.Gln2014=
NM_001368062.3:c.6068A=	NP_001354991.2:p.Gln2023=
NM_001378609.3:c.6203A= MANE Select	NP_001365538.2:p.Gln2068=
NM_001378610.3:c.6203A=	NP_001365539.2:p.Gln2068=
NM_173591.7:c.6203A=	NP_775862.4:p.Gln2068=