Canonical Allele Identifier: CA2049208513

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358750T= , CM000674.2:g.80358750T=	GRCh38
NC_000012.11:g.80752530T= , CM000674.1:g.80752530T=	GRCh37
NC_000012.10:g.79276661T=	NCBI36
NG_033008.1:g.154298T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6201T= MANE Select	ENSP00000447211.2:p.Gly2067=
ENST00000642294.1:c.141T=	ENSP00000493572.1:p.Gly47=
ENST00000646859.1:c.6066T=	ENSP00000496036.1:p.Gly2022=
ENST00000298820.7:c.1502T=
ENST00000458043.6:c.6174T=	ENSP00000400895.2:p.Gly2058=
ENST00000546620.5:n.457T=
ENST00000547103.5:c.6138T=	ENSP00000447211.1:p.Gly2046=
ENST00000550182.2:c.225T=	ENSP00000449641.1:p.Gly75=
ENST00000551340.5:c.329T=
NM_173591.3:c.6174T=	NP_775862.3:p.Gly2058=
XM_005268802.2:c.6225T=	XP_005268859.1:p.Gly2075=
XM_011538191.1:c.6225T=	XP_011536493.1:p.Gly2075=
XM_011538192.1:c.6072T=	XP_011536494.1:p.Gly2024=
XM_011538193.1:c.5859T=	XP_011536495.1:p.Gly1953=
XM_005268802.3:c.6225T=	XP_005268859.1:p.Gly2075=
XM_011538192.2:c.6072T=	XP_011536494.1:p.Gly2024=
NM_001368062.1:c.6039T=	NP_001354991.1:p.Gly2013=
NM_001368062.3:c.6066T=	NP_001354991.2:p.Gly2022=
NM_001378609.3:c.6201T= MANE Select	NP_001365538.2:p.Gly2067=
NM_001378610.3:c.6201T=	NP_001365539.2:p.Gly2067=
NM_173591.7:c.6201T=	NP_775862.4:p.Gly2067=