Canonical Allele Identifier: CA2049208508

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358735A= , CM000674.2:g.80358735A=	GRCh38
NC_000012.11:g.80752515A= , CM000674.1:g.80752515A=	GRCh37
NC_000012.10:g.79276646A=	NCBI36
NG_033008.1:g.154283A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6186A= MANE Select	ENSP00000447211.2:p.Lys2062=
ENST00000642294.1:c.126A=	ENSP00000493572.1:p.Lys42=
ENST00000646859.1:c.6051A=	ENSP00000496036.1:p.Lys2017=
ENST00000298820.7:c.1487A=
ENST00000458043.6:c.6159A=	ENSP00000400895.2:p.Lys2053=
ENST00000546620.5:n.442A=
ENST00000547103.5:c.6123A=	ENSP00000447211.1:p.Lys2041=
ENST00000550182.2:c.210A=	ENSP00000449641.1:p.Lys70=
ENST00000551340.5:c.314A=
NM_173591.3:c.6159A=	NP_775862.3:p.Lys2053=
XM_005268802.2:c.6210A=	XP_005268859.1:p.Lys2070=
XM_011538191.1:c.6210A=	XP_011536493.1:p.Lys2070=
XM_011538192.1:c.6057A=	XP_011536494.1:p.Lys2019=
XM_011538193.1:c.5844A=	XP_011536495.1:p.Lys1948=
XM_005268802.3:c.6210A=	XP_005268859.1:p.Lys2070=
XM_011538192.2:c.6057A=	XP_011536494.1:p.Lys2019=
NM_001368062.1:c.6024A=	NP_001354991.1:p.Lys2008=
NM_001368062.3:c.6051A=	NP_001354991.2:p.Lys2017=
NM_001378609.3:c.6186A= MANE Select	NP_001365538.2:p.Lys2062=
NM_001378610.3:c.6186A=	NP_001365539.2:p.Lys2062=
NM_173591.7:c.6186A=	NP_775862.4:p.Lys2062=