Canonical Allele Identifier: CA379810886

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17574735C>A (hg19) ; chr11:g.17553188C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553188C>A , CM000673.2:g.17553188C>A	GRCh38
NC_000011.9:g.17574735C>A , CM000673.1:g.17574735C>A	GRCh37
NC_000011.8:g.17531311C>A	NCBI36
NG_033191.1:g.10816C>A
NG_033191.2:g.10816C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.398C>A	ENSP00000382323.2:p.Ala133Asp
ENST00000399397.6:c.362C>A MANE Select	ENSP00000382329.2:p.Ala121Asp
ENST00000399391.6:c.398C>A	ENSP00000382323.2:p.Ala133Asp
ENST00000399397.5:c.362C>A	ENSP00000382329.2:p.Ala121Asp
ENST00000428619.1:c.179C>A	ENSP00000399057.2:p.Ala60Asp
ENST00000498332.5:n.268C>A
NM_001277269.1:c.398C>A	NP_001264198.1:p.Ala133Asp
NM_001292063.1:c.362C>A	NP_001278992.1:p.Ala121Asp
NM_001277269.2:c.398C>A	NP_001264198.1:p.Ala133Asp
NM_001292063.2:c.362C>A MANE Select	NP_001278992.1:p.Ala121Asp