Canonical Allele Identifier: CA2049149003

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80229341C= , CM000674.2:g.80229341C=	GRCh38
NC_000012.11:g.80623121C= , CM000674.1:g.80623121C=	GRCh37
NC_000012.10:g.79147252C=	NCBI36
NG_033008.1:g.24889C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.574C= MANE Select	ENSP00000447211.2:p.Arg192=
ENST00000643417.1:n.1234C=
ENST00000646859.1:c.574C=	ENSP00000496036.1:p.Arg192=
ENST00000458043.6:c.547C=	ENSP00000400895.2:p.Arg183=
ENST00000547103.5:c.547C=	ENSP00000447211.1:p.Arg183=
NM_173591.3:c.547C=	NP_775862.3:p.Arg183=
XM_005268802.2:c.598C=	XP_005268859.1:p.Arg200=
XM_011538191.1:c.598C=	XP_011536493.1:p.Arg200=
XM_011538192.1:c.445C=	XP_011536494.1:p.Arg149=
XM_011538193.1:c.232C=	XP_011536495.1:p.Arg78=
XM_005268802.3:c.598C=	XP_005268859.1:p.Arg200=
XM_011538192.2:c.445C=	XP_011536494.1:p.Arg149=
NM_001368062.1:c.547C=	NP_001354991.1:p.Arg183=
NM_001368062.3:c.574C=	NP_001354991.2:p.Arg192=
NM_001378609.3:c.574C= MANE Select	NP_001365538.2:p.Arg192=
NM_001378610.3:c.574C=	NP_001365539.2:p.Arg192=
NM_173591.7:c.574C=	NP_775862.4:p.Arg192=