Canonical Allele Identifier: CA1955197602

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553140G= , CM000673.2:g.17553140G=	GRCh38
NC_000011.9:g.17574687G= , CM000673.1:g.17574687G=	GRCh37
NC_000011.8:g.17531263G=	NCBI36
NG_033191.1:g.10768G=
NG_033191.2:g.10768G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.350G=	ENSP00000382323.2:p.Gly117=
ENST00000399397.6:c.314G= MANE Select	ENSP00000382329.2:p.Gly105=
ENST00000399391.6:c.350G=	ENSP00000382323.2:p.Gly117=
ENST00000399397.5:c.314G=	ENSP00000382329.2:p.Gly105=
ENST00000428619.1:c.131G=	ENSP00000399057.2:p.Gly44=
ENST00000498332.5:n.220G=
NM_001277269.1:c.350G=	NP_001264198.1:p.Gly117=
NM_001292063.1:c.314G=	NP_001278992.1:p.Gly105=
NM_001277269.2:c.350G=	NP_001264198.1:p.Gly117=
NM_001292063.2:c.314G= MANE Select	NP_001278992.1:p.Gly105=