Canonical Allele Identifier: CA473516772

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553444-C-T
• MyVariant Identifiers: chr11:g.17574991C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553444C>T , CM000673.2:g.17553444C>T	GRCh38
NC_000011.9:g.17574991C>T , CM000673.1:g.17574991C>T	GRCh37
NC_000011.8:g.17531567C>T	NCBI36
NG_033191.1:g.11072C>T
NG_033191.2:g.11072C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.501C>T	ENSP00000382323.2:p.Tyr167=
ENST00000399397.6:c.465C>T MANE Select	ENSP00000382329.2:p.Tyr155=
ENST00000399391.6:c.501C>T	ENSP00000382323.2:p.Tyr167=
ENST00000399397.5:c.465C>T	ENSP00000382329.2:p.Tyr155=
ENST00000428619.1:c.282C>T	ENSP00000399057.2:p.Tyr94=
ENST00000498332.5:n.371C>T
NM_001277269.1:c.501C>T	NP_001264198.1:p.Tyr167=
NM_001292063.1:c.465C>T	NP_001278992.1:p.Tyr155=
NM_001277269.2:c.501C>T	NP_001264198.1:p.Tyr167=
NM_001292063.2:c.465C>T MANE Select	NP_001278992.1:p.Tyr155=