Canonical Allele Identifier: CA1955197631

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553198G= , CM000673.2:g.17553198G=	GRCh38
NC_000011.9:g.17574745G= , CM000673.1:g.17574745G=	GRCh37
NC_000011.8:g.17531321G=	NCBI36
NG_033191.1:g.10826G=
NG_033191.2:g.10826G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.408G=	ENSP00000382323.2:p.Pro136=
ENST00000399397.6:c.372G= MANE Select	ENSP00000382329.2:p.Pro124=
ENST00000399391.6:c.408G=	ENSP00000382323.2:p.Pro136=
ENST00000399397.5:c.372G=	ENSP00000382329.2:p.Pro124=
ENST00000428619.1:c.189G=	ENSP00000399057.2:p.Pro63=
ENST00000498332.5:n.278G=
NM_001277269.1:c.408G=	NP_001264198.1:p.Pro136=
NM_001292063.1:c.372G=	NP_001278992.1:p.Pro124=
NM_001277269.2:c.408G=	NP_001264198.1:p.Pro136=
NM_001292063.2:c.372G= MANE Select	NP_001278992.1:p.Pro124=