Canonical Allele Identifier: CA473516727

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17574754G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553207G>A , CM000673.2:g.17553207G>A	GRCh38
NC_000011.9:g.17574754G>A , CM000673.1:g.17574754G>A	GRCh37
NC_000011.8:g.17531330G>A	NCBI36
NG_033191.1:g.10835G>A
NG_033191.2:g.10835G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.417G>A	ENSP00000382323.2:p.Gln139=
ENST00000399397.6:c.381G>A MANE Select	ENSP00000382329.2:p.Gln127=
ENST00000399391.6:c.417G>A	ENSP00000382323.2:p.Gln139=
ENST00000399397.5:c.381G>A	ENSP00000382329.2:p.Gln127=
ENST00000428619.1:c.198G>A	ENSP00000399057.2:p.Gln66=
ENST00000498332.5:n.287G>A
NM_001277269.1:c.417G>A	NP_001264198.1:p.Gln139=
NM_001292063.1:c.381G>A	NP_001278992.1:p.Gln127=
NM_001277269.2:c.417G>A	NP_001264198.1:p.Gln139=
NM_001292063.2:c.381G>A MANE Select	NP_001278992.1:p.Gln127=