Canonical Allele Identifier: CA473516755

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553411-G-T
• MyVariant Identifiers: chr11:g.17574958G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553411G>T , CM000673.2:g.17553411G>T	GRCh38
NC_000011.9:g.17574958G>T , CM000673.1:g.17574958G>T	GRCh37
NC_000011.8:g.17531534G>T	NCBI36
NG_033191.1:g.11039G>T
NG_033191.2:g.11039G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.468G>T	ENSP00000382323.2:p.Gly156=
ENST00000399397.6:c.432G>T MANE Select	ENSP00000382329.2:p.Gly144=
ENST00000399391.6:c.468G>T	ENSP00000382323.2:p.Gly156=
ENST00000399397.5:c.432G>T	ENSP00000382329.2:p.Gly144=
ENST00000428619.1:c.249G>T	ENSP00000399057.2:p.Gly83=
ENST00000498332.5:n.338G>T
NM_001277269.1:c.468G>T	NP_001264198.1:p.Gly156=
NM_001292063.1:c.432G>T	NP_001278992.1:p.Gly144=
NM_001277269.2:c.468G>T	NP_001264198.1:p.Gly156=
NM_001292063.2:c.432G>T MANE Select	NP_001278992.1:p.Gly144=