Canonical Allele Identifier: CA473516687

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17574688A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553141A>T , CM000673.2:g.17553141A>T	GRCh38
NC_000011.9:g.17574688A>T , CM000673.1:g.17574688A>T	GRCh37
NC_000011.8:g.17531264A>T	NCBI36
NG_033191.1:g.10769A>T
NG_033191.2:g.10769A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.351A>T	ENSP00000382323.2:p.Gly117=
ENST00000399397.6:c.315A>T MANE Select	ENSP00000382329.2:p.Gly105=
ENST00000399391.6:c.351A>T	ENSP00000382323.2:p.Gly117=
ENST00000399397.5:c.315A>T	ENSP00000382329.2:p.Gly105=
ENST00000428619.1:c.132A>T	ENSP00000399057.2:p.Gly44=
ENST00000498332.5:n.221A>T
NM_001277269.1:c.351A>T	NP_001264198.1:p.Gly117=
NM_001292063.1:c.315A>T	NP_001278992.1:p.Gly105=
NM_001277269.2:c.351A>T	NP_001264198.1:p.Gly117=
NM_001292063.2:c.315A>T MANE Select	NP_001278992.1:p.Gly105=