Canonical Allele Identifier: CA218490106

Gene: OTOG

Linked Data

• dbSNP Id: rs1040999212
• MyVariant Identifiers: chr11:g.17574935G>A (hg19) ; chr11:g.17553388G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553388G>A , CM000673.2:g.17553388G>A	GRCh38
NC_000011.9:g.17574935G>A , CM000673.1:g.17574935G>A	GRCh37
NC_000011.8:g.17531511G>A	NCBI36
NG_033191.1:g.11016G>A
NG_033191.2:g.11016G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399391.7:c.445G>A	ENSP00000382323.2:p.Asp149Asn
ENST00000399397.6:c.409G>A MANE Select	ENSP00000382329.2:p.Asp137Asn
ENST00000399391.6:c.445G>A	ENSP00000382323.2:p.Asp149Asn
ENST00000399397.5:c.409G>A	ENSP00000382329.2:p.Asp137Asn
ENST00000428619.1:c.226G>A	ENSP00000399057.2:p.Asp76Asn
ENST00000498332.5:n.315G>A
NM_001277269.1:c.445G>A	NP_001264198.1:p.Asp149Asn
NM_001292063.1:c.409G>A	NP_001278992.1:p.Asp137Asn
NM_001277269.2:c.445G>A	NP_001264198.1:p.Asp149Asn
NM_001292063.2:c.409G>A MANE Select	NP_001278992.1:p.Asp137Asn