Canonical Allele Identifier: CA2612686774

Gene: OTOG

Linked Data

• gnomAD v4: 11-17612611-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612611C>G , CM000673.2:g.17612611C>G	GRCh38
NC_000011.9:g.17634158C>G , CM000673.1:g.17634158C>G	GRCh37
NC_000011.8:g.17590734C>G	NCBI36
NG_033191.1:g.70239C>G
NG_033191.2:g.70239C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6329-9C>G	ENSP00000382323.2:n.6329-9C>G
ENST00000399397.6:c.6293-9C>G MANE Select	ENSP00000382329.2:n.6293-9C>G
ENST00000342528.2:c.3347-9C>G	ENSP00000341666.2:n.3347-9C>G
ENST00000399391.6:c.6329-9C>G	ENSP00000382323.2:n.6329-9C>G
ENST00000399397.5:c.6293-9C>G	ENSP00000382329.2:n.6293-9C>G
NM_001277269.1:c.6329-9C>G	NP_001264198.1:n.6329-9C>G
NM_001292063.1:c.6293-9C>G	NP_001278992.1:n.6293-9C>G
NM_001277269.2:c.6329-9C>G	NP_001264198.1:n.6329-9C>G
NM_001292063.2:c.6293-9C>G MANE Select	NP_001278992.1:n.6293-9C>G