Canonical Allele Identifier: CA473518235

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17631911G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17610364G>A , CM000673.2:g.17610364G>A	GRCh38
NC_000011.9:g.17631911G>A , CM000673.1:g.17631911G>A	GRCh37
NC_000011.8:g.17588487G>A	NCBI36
NG_033191.1:g.67992G>A
NG_033191.2:g.67992G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399391.7:c.5100G>A	ENSP00000382323.2:p.Gln1700=
ENST00000399397.6:c.5064G>A MANE Select	ENSP00000382329.2:p.Gln1688=
ENST00000342528.2:c.2118G>A	ENSP00000341666.2:p.Gln706=
ENST00000399391.6:c.5100G>A	ENSP00000382323.2:p.Gln1700=
ENST00000399397.5:c.5064G>A	ENSP00000382329.2:p.Gln1688=
NM_001277269.1:c.5100G>A	NP_001264198.1:p.Gln1700=
NM_001292063.1:c.5064G>A	NP_001278992.1:p.Gln1688=
NM_001277269.2:c.5100G>A	NP_001264198.1:p.Gln1700=
NM_001292063.2:c.5064G>A MANE Select	NP_001278992.1:p.Gln1688=