Canonical Allele Identifier: CA1955236977

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635187G= , CM000673.2:g.17635187G=	GRCh38
NC_000011.9:g.17656734G= , CM000673.1:g.17656734G=	GRCh37
NC_000011.8:g.17613310G=	NCBI36
NG_033191.1:g.92815G=
NG_033191.2:g.92815G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729G=	ENSP00000382323.2:p.Ala2577=
ENST00000399397.6:c.7693G= MANE Select	ENSP00000382329.2:p.Ala2565=
ENST00000342528.2:c.4322-423G=	ENSP00000341666.2:n.4322-423G=
ENST00000399391.6:c.7729G=	ENSP00000382323.2:p.Ala2577=
ENST00000399397.5:c.7693G=	ENSP00000382329.2:p.Ala2565=
NM_001277269.1:c.7729G=	NP_001264198.1:p.Ala2577=
NM_001292063.1:c.7693G=	NP_001278992.1:p.Ala2565=
NM_001277269.2:c.7729G=	NP_001264198.1:p.Ala2577=
NM_001292063.2:c.7693G= MANE Select	NP_001278992.1:p.Ala2565=