Canonical Allele Identifier: CA379810875

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17574733T>G (hg19) ; chr11:g.17553186T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553186T>G , CM000673.2:g.17553186T>G	GRCh38
NC_000011.9:g.17574733T>G , CM000673.1:g.17574733T>G	GRCh37
NC_000011.8:g.17531309T>G	NCBI36
NG_033191.1:g.10814T>G
NG_033191.2:g.10814T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.396T>G	ENSP00000382323.2:p.Asn132Lys
ENST00000399397.6:c.360T>G MANE Select	ENSP00000382329.2:p.Asn120Lys
ENST00000399391.6:c.396T>G	ENSP00000382323.2:p.Asn132Lys
ENST00000399397.5:c.360T>G	ENSP00000382329.2:p.Asn120Lys
ENST00000428619.1:c.177T>G	ENSP00000399057.2:p.Asn59Lys
ENST00000498332.5:n.266T>G
NM_001277269.1:c.396T>G	NP_001264198.1:p.Asn132Lys
NM_001292063.1:c.360T>G	NP_001278992.1:p.Asn120Lys
NM_001277269.2:c.396T>G	NP_001264198.1:p.Asn132Lys
NM_001292063.2:c.360T>G MANE Select	NP_001278992.1:p.Asn120Lys