Canonical Allele Identifier: CA5905348

Gene: OTOG

Linked Data

• dbSNP Id: rs532369279
• ExAC: 11:17574865 G / A
• gnomAD v2: 11-17574865-G-A
• gnomAD v3: 11-17553318-G-A
• gnomAD v4: 11-17553318-G-A
• MyVariant Identifiers: chr11:g.17574865G>A (hg19) ; chr11:g.17553318G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553318G>A , CM000673.2:g.17553318G>A	GRCh38
NC_000011.9:g.17574865G>A , CM000673.1:g.17574865G>A	GRCh37
NC_000011.8:g.17531441G>A	NCBI36
NG_033191.1:g.10946G>A
NG_033191.2:g.10946G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.422-47G>A	ENSP00000382323.2:n.422-47G>A
ENST00000399397.6:c.386-47G>A MANE Select	ENSP00000382329.2:n.386-47G>A
ENST00000399391.6:c.422-47G>A	ENSP00000382323.2:n.422-47G>A
ENST00000399397.5:c.386-47G>A	ENSP00000382329.2:n.386-47G>A
ENST00000428619.1:c.203-47G>A	ENSP00000399057.2:n.203-47G>A
ENST00000498332.5:n.292-47G>A
NM_001277269.1:c.422-47G>A	NP_001264198.1:n.422-47G>A
NM_001292063.1:c.386-47G>A	NP_001278992.1:n.386-47G>A
NM_001277269.2:c.422-47G>A	NP_001264198.1:n.422-47G>A
NM_001292063.2:c.386-47G>A MANE Select	NP_001278992.1:n.386-47G>A