Canonical Allele Identifier: CA379811468

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553427-A-T
• MyVariant Identifiers: chr11:g.17574974A>T (hg19) ; chr11:g.17553427A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553427A>T , CM000673.2:g.17553427A>T	GRCh38
NC_000011.9:g.17574974A>T , CM000673.1:g.17574974A>T	GRCh37
NC_000011.8:g.17531550A>T	NCBI36
NG_033191.1:g.11055A>T
NG_033191.2:g.11055A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.484A>T	ENSP00000382323.2:p.Thr162Ser
ENST00000399397.6:c.448A>T MANE Select	ENSP00000382329.2:p.Thr150Ser
ENST00000399391.6:c.484A>T	ENSP00000382323.2:p.Thr162Ser
ENST00000399397.5:c.448A>T	ENSP00000382329.2:p.Thr150Ser
ENST00000428619.1:c.265A>T	ENSP00000399057.2:p.Thr89Ser
ENST00000498332.5:n.354A>T
NM_001277269.1:c.484A>T	NP_001264198.1:p.Thr162Ser
NM_001292063.1:c.448A>T	NP_001278992.1:p.Thr150Ser
NM_001277269.2:c.484A>T	NP_001264198.1:p.Thr162Ser
NM_001292063.2:c.448A>T MANE Select	NP_001278992.1:p.Thr150Ser