Canonical Allele Identifier: CA1955197601

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553138T= , CM000673.2:g.17553138T=	GRCh38
NC_000011.9:g.17574685T= , CM000673.1:g.17574685T=	GRCh37
NC_000011.8:g.17531261T=	NCBI36
NG_033191.1:g.10766T=
NG_033191.2:g.10766T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.348T=	ENSP00000382323.2:p.Asn116=
ENST00000399397.6:c.312T= MANE Select	ENSP00000382329.2:p.Asn104=
ENST00000399391.6:c.348T=	ENSP00000382323.2:p.Asn116=
ENST00000399397.5:c.312T=	ENSP00000382329.2:p.Asn104=
ENST00000428619.1:c.129T=	ENSP00000399057.2:p.Asn43=
ENST00000498332.5:n.218T=
NM_001277269.1:c.348T=	NP_001264198.1:p.Asn116=
NM_001292063.1:c.312T=	NP_001278992.1:p.Asn104=
NM_001277269.2:c.348T=	NP_001264198.1:p.Asn116=
NM_001292063.2:c.312T= MANE Select	NP_001278992.1:p.Asn104=