Canonical Allele Identifier: CA1955197666

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553238A= , CM000673.2:g.17553238A=	GRCh38
NC_000011.9:g.17574785A= , CM000673.1:g.17574785A=	GRCh37
NC_000011.8:g.17531361A=	NCBI36
NG_033191.1:g.10866A=
NG_033191.2:g.10866A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.421+27A=	ENSP00000382323.2:n.421+27A=
ENST00000399397.6:c.385+27A= MANE Select	ENSP00000382329.2:n.385+27A=
ENST00000399391.6:c.421+27A=	ENSP00000382323.2:n.421+27A=
ENST00000399397.5:c.385+27A=	ENSP00000382329.2:n.385+27A=
ENST00000428619.1:c.202+27A=	ENSP00000399057.2:n.202+27A=
ENST00000498332.5:n.291+27A=
NM_001277269.1:c.421+27A=	NP_001264198.1:n.421+27A=
NM_001292063.1:c.385+27A=	NP_001278992.1:n.385+27A=
NM_001277269.2:c.421+27A=	NP_001264198.1:n.421+27A=
NM_001292063.2:c.385+27A= MANE Select	NP_001278992.1:n.385+27A=