Canonical Allele Identifier: CA2612679158

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553034-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553035dup , CM000673.2:g.17553035dup	GRCh38
NC_000011.9:g.17574582dup , CM000673.1:g.17574582dup	GRCh37
NC_000011.8:g.17531158dup	NCBI36
NG_033191.1:g.10663dup
NG_033191.2:g.10663dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.329-84dup	ENSP00000382323.2:n.329-84dup
ENST00000399397.6:c.293-84dup MANE Select	ENSP00000382329.2:n.293-84dup
ENST00000399391.6:c.329-84dup	ENSP00000382323.2:n.329-84dup
ENST00000399397.5:c.293-84dup	ENSP00000382329.2:n.293-84dup
ENST00000428619.1:c.110-84dup	ENSP00000399057.2:n.110-84dup
ENST00000498332.5:n.199-84dup
NM_001277269.1:c.329-84dup	NP_001264198.1:n.329-84dup
NM_001292063.1:c.293-84dup	NP_001278992.1:n.293-84dup
NM_001277269.2:c.329-84dup	NP_001264198.1:n.329-84dup
NM_001292063.2:c.293-84dup MANE Select	NP_001278992.1:n.293-84dup