Canonical Allele Identifier: CA1955236948

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635140T= , CM000673.2:g.17635140T=	GRCh38
NC_000011.9:g.17656687T= , CM000673.1:g.17656687T=	GRCh37
NC_000011.8:g.17613263T=	NCBI36
NG_033191.1:g.92768T=
NG_033191.2:g.92768T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7682T=	ENSP00000382323.2:p.Leu2561=
ENST00000399397.6:c.7646T= MANE Select	ENSP00000382329.2:p.Leu2549=
ENST00000342528.2:c.4322-470T=	ENSP00000341666.2:n.4322-470T=
ENST00000399391.6:c.7682T=	ENSP00000382323.2:p.Leu2561=
ENST00000399397.5:c.7646T=	ENSP00000382329.2:p.Leu2549=
NM_001277269.1:c.7682T=	NP_001264198.1:p.Leu2561=
NM_001292063.1:c.7646T=	NP_001278992.1:p.Leu2549=
NM_001277269.2:c.7682T=	NP_001264198.1:p.Leu2561=
NM_001292063.2:c.7646T= MANE Select	NP_001278992.1:p.Leu2549=