Canonical Allele Identifier: CA473516706

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17574724A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553177A>G , CM000673.2:g.17553177A>G	GRCh38
NC_000011.9:g.17574724A>G , CM000673.1:g.17574724A>G	GRCh37
NC_000011.8:g.17531300A>G	NCBI36
NG_033191.1:g.10805A>G
NG_033191.2:g.10805A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.387A>G	ENSP00000382323.2:p.Arg129=
ENST00000399397.6:c.351A>G MANE Select	ENSP00000382329.2:p.Arg117=
ENST00000399391.6:c.387A>G	ENSP00000382323.2:p.Arg129=
ENST00000399397.5:c.351A>G	ENSP00000382329.2:p.Arg117=
ENST00000428619.1:c.168A>G	ENSP00000399057.2:p.Arg56=
ENST00000498332.5:n.257A>G
NM_001277269.1:c.387A>G	NP_001264198.1:p.Arg129=
NM_001292063.1:c.351A>G	NP_001278992.1:p.Arg117=
NM_001277269.2:c.387A>G	NP_001264198.1:p.Arg129=
NM_001292063.2:c.351A>G MANE Select	NP_001278992.1:p.Arg117=