Canonical Allele Identifier: CA2049208581

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358893G= , CM000674.2:g.80358893G=	GRCh38
NC_000012.11:g.80752673G= , CM000674.1:g.80752673G=	GRCh37
NC_000012.10:g.79276804G=	NCBI36
NG_033008.1:g.154441G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6260G= MANE Select	ENSP00000447211.2:p.Cys2087=
ENST00000642294.1:c.200G=	ENSP00000493572.1:p.Cys67=
ENST00000646859.1:c.6125G=	ENSP00000496036.1:p.Cys2042=
ENST00000298820.7:c.1527+118G=
ENST00000458043.6:c.6233G=	ENSP00000400895.2:p.Cys2078=
ENST00000546620.5:n.516G=
ENST00000547103.5:c.6197G=	ENSP00000447211.1:p.Cys2066=
ENST00000550182.2:c.284G=	ENSP00000449641.1:p.Cys95=
ENST00000551340.5:c.388G=
NM_173591.3:c.6233G=	NP_775862.3:p.Cys2078=
XM_005268802.2:c.6284G=	XP_005268859.1:p.Cys2095=
XM_011538191.1:c.6284G=	XP_011536493.1:p.Cys2095=
XM_011538192.1:c.6131G=	XP_011536494.1:p.Cys2044=
XM_011538193.1:c.5918G=	XP_011536495.1:p.Cys1973=
XM_005268802.3:c.6284G=	XP_005268859.1:p.Cys2095=
XM_011538192.2:c.6131G=	XP_011536494.1:p.Cys2044=
NM_001368062.1:c.6098G=	NP_001354991.1:p.Cys2033=
NM_001368062.3:c.6125G=	NP_001354991.2:p.Cys2042=
NM_001378609.3:c.6260G= MANE Select	NP_001365538.2:p.Cys2087=
NM_001378610.3:c.6260G=	NP_001365539.2:p.Cys2087=
NM_173591.7:c.6260G=	NP_775862.4:p.Cys2087=