Canonical Allele Identifier: CA2612690398

Gene: OTOG

Linked Data

• gnomAD v4: 11-17635306-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635306G>T , CM000673.2:g.17635306G>T	GRCh38
NC_000011.9:g.17656853G>T , CM000673.1:g.17656853G>T	GRCh37
NC_000011.8:g.17613429G>T	NCBI36
NG_033191.1:g.92934G>T
NG_033191.2:g.92934G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+119G>T	ENSP00000382323.2:n.7729+119G>T
ENST00000399397.6:c.7693+119G>T MANE Select	ENSP00000382329.2:n.7693+119G>T
ENST00000342528.2:c.4322-304G>T	ENSP00000341666.2:n.4322-304G>T
ENST00000399391.6:c.7729+119G>T	ENSP00000382323.2:n.7729+119G>T
ENST00000399397.5:c.7693+119G>T	ENSP00000382329.2:n.7693+119G>T
NM_001277269.1:c.7729+119G>T	NP_001264198.1:n.7729+119G>T
NM_001292063.1:c.7693+119G>T	NP_001278992.1:n.7693+119G>T
NM_001277269.2:c.7729+119G>T	NP_001264198.1:n.7729+119G>T
NM_001292063.2:c.7693+119G>T MANE Select	NP_001278992.1:n.7693+119G>T