Canonical Allele Identifier: CA473305692

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17634168C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612621C>T , CM000673.2:g.17612621C>T	GRCh38
NC_000011.9:g.17634168C>T , CM000673.1:g.17634168C>T	GRCh37
NC_000011.8:g.17590744C>T	NCBI36
NG_033191.1:g.70249C>T
NG_033191.2:g.70249C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6330C>T	ENSP00000382323.2:p.Cys2110=
ENST00000399397.6:c.6294C>T MANE Select	ENSP00000382329.2:p.Cys2098=
ENST00000342528.2:c.3348C>T	ENSP00000341666.2:p.Cys1116=
ENST00000399391.6:c.6330C>T	ENSP00000382323.2:p.Cys2110=
ENST00000399397.5:c.6294C>T	ENSP00000382329.2:p.Cys2098=
NM_001277269.1:c.6330C>T	NP_001264198.1:p.Cys2110=
NM_001292063.1:c.6294C>T	NP_001278992.1:p.Cys2098=
NM_001277269.2:c.6330C>T	NP_001264198.1:p.Cys2110=
NM_001292063.2:c.6294C>T MANE Select	NP_001278992.1:p.Cys2098=