Canonical Allele Identifier: CA2612678990

Gene: OTOG

Linked Data

• gnomAD v4: 11-17552992-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17552992C>G , CM000673.2:g.17552992C>G	GRCh38
NC_000011.9:g.17574539C>G , CM000673.1:g.17574539C>G	GRCh37
NC_000011.8:g.17531115C>G	NCBI36
NG_033191.1:g.10620C>G
NG_033191.2:g.10620C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.329-127C>G	ENSP00000382323.2:n.329-127C>G
ENST00000399397.6:c.293-127C>G MANE Select	ENSP00000382329.2:n.293-127C>G
ENST00000399391.6:c.329-127C>G	ENSP00000382323.2:n.329-127C>G
ENST00000399397.5:c.293-127C>G	ENSP00000382329.2:n.293-127C>G
ENST00000428619.1:c.110-127C>G	ENSP00000399057.2:n.110-127C>G
ENST00000498332.5:n.199-127C>G
NM_001277269.1:c.329-127C>G	NP_001264198.1:n.329-127C>G
NM_001292063.1:c.293-127C>G	NP_001278992.1:n.293-127C>G
NM_001277269.2:c.329-127C>G	NP_001264198.1:n.329-127C>G
NM_001292063.2:c.293-127C>G MANE Select	NP_001278992.1:n.293-127C>G