Canonical Allele Identifier: CA473516782

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17575006A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553459A>T , CM000673.2:g.17553459A>T	GRCh38
NC_000011.9:g.17575006A>T , CM000673.1:g.17575006A>T	GRCh37
NC_000011.8:g.17531582A>T	NCBI36
NG_033191.1:g.11087A>T
NG_033191.2:g.11087A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.516A>T	ENSP00000382323.2:p.Gly172=
ENST00000399397.6:c.480A>T MANE Select	ENSP00000382329.2:p.Gly160=
ENST00000399391.6:c.516A>T	ENSP00000382323.2:p.Gly172=
ENST00000399397.5:c.480A>T	ENSP00000382329.2:p.Gly160=
ENST00000498332.5:n.386A>T
NM_001277269.1:c.516A>T	NP_001264198.1:p.Gly172=
NM_001292063.1:c.480A>T	NP_001278992.1:p.Gly160=
NM_001277269.2:c.516A>T	NP_001264198.1:p.Gly172=
NM_001292063.2:c.480A>T MANE Select	NP_001278992.1:p.Gly160=