Canonical Allele Identifier: CA674252762
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17606016del , CM000673.2:g.17606016del GRCh38
NC_000011.9:g.17627563del , CM000673.1:g.17627563del GRCh37
NC_000011.8:g.17584139del NCBI36
NG_033191.1:g.63644del
NG_033191.2:g.63644del

Transcript Alleles

HGVS Amino-acid Change
NM_001292063.2:c.4037del MANE Select NP_001278992.1:p.Val1346GlyfsTer?
ENST00000399397.6:c.4037del MANE Select ENSP00000382329.2:p.Val1346GlyfsTer?
NM_001277269.1:c.4073del NP_001264198.1:p.Val1358GlyfsTer?
NM_001277269.2:c.4073del NP_001264198.1:p.Val1358GlyfsTer?
NM_001292063.1:c.4037del NP_001278992.1:p.Val1346GlyfsTer?
ENST00000342528.2:c.1091del ENSP00000341666.2:p.Val364GlyfsTer?
ENST00000399391.6:c.4073del ENSP00000382323.2:p.Val1358GlyfsTer?
ENST00000399391.7:c.4073del ENSP00000382323.2:p.Val1358GlyfsTer?
ENST00000399397.5:c.4037del ENSP00000382329.2:p.Val1346GlyfsTer?