Canonical Allele Identifier: CA2049207226

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80355885C= , CM000674.2:g.80355885C=	GRCh38
NC_000012.11:g.80749665C= , CM000674.1:g.80749665C=	GRCh37
NC_000012.10:g.79273796C=	NCBI36
NG_033008.1:g.151433C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.5743C= MANE Select	ENSP00000447211.2:p.Arg1915=
ENST00000646859.1:c.5608C=	ENSP00000496036.1:p.Arg1870=
ENST00000298820.7:c.1044C=
ENST00000458043.6:c.5716C=	ENSP00000400895.2:p.Arg1906=
ENST00000547103.5:c.5680C=	ENSP00000447211.1:p.Arg1894=
NM_173591.3:c.5716C=	NP_775862.3:p.Arg1906=
XM_005268802.2:c.5767C=	XP_005268859.1:p.Arg1923=
XM_011538191.1:c.5767C=	XP_011536493.1:p.Arg1923=
XM_011538192.1:c.5614C=	XP_011536494.1:p.Arg1872=
XM_011538193.1:c.5401C=	XP_011536495.1:p.Arg1801=
XM_005268802.3:c.5767C=	XP_005268859.1:p.Arg1923=
XM_011538192.2:c.5614C=	XP_011536494.1:p.Arg1872=
NM_001368062.1:c.5581C=	NP_001354991.1:p.Arg1861=
NM_001368062.3:c.5608C=	NP_001354991.2:p.Arg1870=
NM_001378609.3:c.5743C= MANE Select	NP_001365538.2:p.Arg1915=
NM_001378610.3:c.5743C=	NP_001365539.2:p.Arg1915=
NM_173591.7:c.5743C=	NP_775862.4:p.Arg1915=