Canonical Allele Identifier: CA473305608

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17633843T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612296T>C , CM000673.2:g.17612296T>C	GRCh38
NC_000011.9:g.17633843T>C , CM000673.1:g.17633843T>C	GRCh37
NC_000011.8:g.17590419T>C	NCBI36
NG_033191.1:g.69924T>C
NG_033191.2:g.69924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6294T>C	ENSP00000382323.2:p.Gly2098=
ENST00000399397.6:c.6258T>C MANE Select	ENSP00000382329.2:p.Gly2086=
ENST00000342528.2:c.3312T>C	ENSP00000341666.2:p.Gly1104=
ENST00000399391.6:c.6294T>C	ENSP00000382323.2:p.Gly2098=
ENST00000399397.5:c.6258T>C	ENSP00000382329.2:p.Gly2086=
NM_001277269.1:c.6294T>C	NP_001264198.1:p.Gly2098=
NM_001292063.1:c.6258T>C	NP_001278992.1:p.Gly2086=
NM_001277269.2:c.6294T>C	NP_001264198.1:p.Gly2098=
NM_001292063.2:c.6258T>C MANE Select	NP_001278992.1:p.Gly2086=