Canonical Allele Identifier: CA379804524

Gene: OTOG

Linked Data

• gnomAD v3: 11-17612733-G-T
• gnomAD v4: 11-17612733-G-T
• MyVariant Identifiers: chr11:g.17634280G>T (hg19) ; chr11:g.17612733G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612733G>T , CM000673.2:g.17612733G>T	GRCh38
NC_000011.9:g.17634280G>T , CM000673.1:g.17634280G>T	GRCh37
NC_000011.8:g.17590856G>T	NCBI36
NG_033191.1:g.70361G>T
NG_033191.2:g.70361G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6442G>T	ENSP00000382323.2:p.Val2148Phe
ENST00000399397.6:c.6406G>T MANE Select	ENSP00000382329.2:p.Val2136Phe
ENST00000342528.2:c.3460G>T	ENSP00000341666.2:p.Val1154Phe
ENST00000399391.6:c.6442G>T	ENSP00000382323.2:p.Val2148Phe
ENST00000399397.5:c.6406G>T	ENSP00000382329.2:p.Val2136Phe
NM_001277269.1:c.6442G>T	NP_001264198.1:p.Val2148Phe
NM_001292063.1:c.6406G>T	NP_001278992.1:p.Val2136Phe
NM_001277269.2:c.6442G>T	NP_001264198.1:p.Val2148Phe
NM_001292063.2:c.6406G>T MANE Select	NP_001278992.1:p.Val2136Phe