Canonical Allele Identifier: CA1955197793
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553478G= , CM000673.2:g.17553478G= GRCh38
NC_000011.9:g.17575025G= , CM000673.1:g.17575025G= GRCh37
NC_000011.8:g.17531601G= NCBI36
NG_033191.1:g.11106G=
NG_033191.2:g.11106G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.535G= ENSP00000382323.2:p.Val179=
ENST00000399397.6:c.499G= MANE Select ENSP00000382329.2:p.Val167=
ENST00000399391.6:c.535G= ENSP00000382323.2:p.Val179=
ENST00000399397.5:c.499G= ENSP00000382329.2:p.Val167=
ENST00000498332.5:n.405G=
NM_001277269.1:c.535G= NP_001264198.1:p.Val179=
NM_001292063.1:c.499G= NP_001278992.1:p.Val167=
NM_001277269.2:c.535G= NP_001264198.1:p.Val179=
NM_001292063.2:c.499G= MANE Select NP_001278992.1:p.Val167=