Canonical Allele Identifier: CA379810892

Gene: OTOG

Linked Data

• dbSNP Id: rs1410432017
• gnomAD v2: 11-17574735-C-T
• MyVariant Identifiers: chr11:g.17574735C>T (hg19) ; chr11:g.17553188C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553188C>T , CM000673.2:g.17553188C>T	GRCh38
NC_000011.9:g.17574735C>T , CM000673.1:g.17574735C>T	GRCh37
NC_000011.8:g.17531311C>T	NCBI36
NG_033191.1:g.10816C>T
NG_033191.2:g.10816C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.398C>T	ENSP00000382323.2:p.Ala133Val
ENST00000399397.6:c.362C>T MANE Select	ENSP00000382329.2:p.Ala121Val
ENST00000399391.6:c.398C>T	ENSP00000382323.2:p.Ala133Val
ENST00000399397.5:c.362C>T	ENSP00000382329.2:p.Ala121Val
ENST00000428619.1:c.179C>T	ENSP00000399057.2:p.Ala60Val
ENST00000498332.5:n.268C>T
NM_001277269.1:c.398C>T	NP_001264198.1:p.Ala133Val
NM_001292063.1:c.362C>T	NP_001278992.1:p.Ala121Val
NM_001277269.2:c.398C>T	NP_001264198.1:p.Ala133Val
NM_001292063.2:c.362C>T MANE Select	NP_001278992.1:p.Ala121Val