Canonical Allele Identifier: CA1955197762

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553419A= , CM000673.2:g.17553419A=	GRCh38
NC_000011.9:g.17574966A= , CM000673.1:g.17574966A=	GRCh37
NC_000011.8:g.17531542A=	NCBI36
NG_033191.1:g.11047A=
NG_033191.2:g.11047A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.476A=	ENSP00000382323.2:p.His159=
ENST00000399397.6:c.440A= MANE Select	ENSP00000382329.2:p.His147=
ENST00000399391.6:c.476A=	ENSP00000382323.2:p.His159=
ENST00000399397.5:c.440A=	ENSP00000382329.2:p.His147=
ENST00000428619.1:c.257A=	ENSP00000399057.2:p.His86=
ENST00000498332.5:n.346A=
NM_001277269.1:c.476A=	NP_001264198.1:p.His159=
NM_001292063.1:c.440A=	NP_001278992.1:p.His147=
NM_001277269.2:c.476A=	NP_001264198.1:p.His159=
NM_001292063.2:c.440A= MANE Select	NP_001278992.1:p.His147=