Canonical Allele Identifier: CA2612678939

Gene: OTOG

Linked Data

• gnomAD v4: 11-17552970-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17552970A>T , CM000673.2:g.17552970A>T	GRCh38
NC_000011.9:g.17574517A>T , CM000673.1:g.17574517A>T	GRCh37
NC_000011.8:g.17531093A>T	NCBI36
NG_033191.1:g.10598A>T
NG_033191.2:g.10598A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.329-149A>T	ENSP00000382323.2:n.329-149A>T
ENST00000399397.6:c.293-149A>T MANE Select	ENSP00000382329.2:n.293-149A>T
ENST00000399391.6:c.329-149A>T	ENSP00000382323.2:n.329-149A>T
ENST00000399397.5:c.293-149A>T	ENSP00000382329.2:n.293-149A>T
ENST00000428619.1:c.110-149A>T	ENSP00000399057.2:n.110-149A>T
ENST00000498332.5:n.199-149A>T
NM_001277269.1:c.329-149A>T	NP_001264198.1:n.329-149A>T
NM_001292063.1:c.293-149A>T	NP_001278992.1:n.293-149A>T
NM_001277269.2:c.329-149A>T	NP_001264198.1:n.329-149A>T
NM_001292063.2:c.293-149A>T MANE Select	NP_001278992.1:n.293-149A>T