Canonical Allele Identifier: CA1955197741

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553376G= , CM000673.2:g.17553376G=	GRCh38
NC_000011.9:g.17574923G= , CM000673.1:g.17574923G=	GRCh37
NC_000011.8:g.17531499G=	NCBI36
NG_033191.1:g.11004G=
NG_033191.2:g.11004G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.433G=	ENSP00000382323.2:p.Gly145=
ENST00000399397.6:c.397G= MANE Select	ENSP00000382329.2:p.Gly133=
ENST00000399391.6:c.433G=	ENSP00000382323.2:p.Gly145=
ENST00000399397.5:c.397G=	ENSP00000382329.2:p.Gly133=
ENST00000428619.1:c.214G=	ENSP00000399057.2:p.Gly72=
ENST00000498332.5:n.303G=
NM_001277269.1:c.433G=	NP_001264198.1:p.Gly145=
NM_001292063.1:c.397G=	NP_001278992.1:p.Gly133=
NM_001277269.2:c.433G=	NP_001264198.1:p.Gly145=
NM_001292063.2:c.397G= MANE Select	NP_001278992.1:p.Gly133=