Canonical Allele Identifier: CA473516697

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17574706A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553159A>G , CM000673.2:g.17553159A>G	GRCh38
NC_000011.9:g.17574706A>G , CM000673.1:g.17574706A>G	GRCh37
NC_000011.8:g.17531282A>G	NCBI36
NG_033191.1:g.10787A>G
NG_033191.2:g.10787A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.369A>G	ENSP00000382323.2:p.Pro123=
ENST00000399397.6:c.333A>G MANE Select	ENSP00000382329.2:p.Pro111=
ENST00000399391.6:c.369A>G	ENSP00000382323.2:p.Pro123=
ENST00000399397.5:c.333A>G	ENSP00000382329.2:p.Pro111=
ENST00000428619.1:c.150A>G	ENSP00000399057.2:p.Pro50=
ENST00000498332.5:n.239A>G
NM_001277269.1:c.369A>G	NP_001264198.1:p.Pro123=
NM_001292063.1:c.333A>G	NP_001278992.1:p.Pro111=
NM_001277269.2:c.369A>G	NP_001264198.1:p.Pro123=
NM_001292063.2:c.333A>G MANE Select	NP_001278992.1:p.Pro111=