Canonical Allele Identifier: CA379812722

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17656461C>G (hg19) ; chr11:g.17634914C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634914C>G , CM000673.2:g.17634914C>G	GRCh38
NC_000011.9:g.17656461C>G , CM000673.1:g.17656461C>G	GRCh37
NC_000011.8:g.17613037C>G	NCBI36
NG_033191.1:g.92542C>G
NG_033191.2:g.92542C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7587C>G	ENSP00000382323.2:p.Phe2529Leu
ENST00000399397.6:c.7551C>G MANE Select	ENSP00000382329.2:p.Phe2517Leu
ENST00000342528.2:c.4322-696C>G	ENSP00000341666.2:n.4322-696C>G
ENST00000399391.6:c.7587C>G	ENSP00000382323.2:p.Phe2529Leu
ENST00000399397.5:c.7551C>G	ENSP00000382329.2:p.Phe2517Leu
NM_001277269.1:c.7587C>G	NP_001264198.1:p.Phe2529Leu
NM_001292063.1:c.7551C>G	NP_001278992.1:p.Phe2517Leu
NM_001277269.2:c.7587C>G	NP_001264198.1:p.Phe2529Leu
NM_001292063.2:c.7551C>G MANE Select	NP_001278992.1:p.Phe2517Leu