Canonical Allele Identifier: CA1955237003
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17635232G= , CM000673.2:g.17635232G= GRCh38
NC_000011.9:g.17656779G= , CM000673.1:g.17656779G= GRCh37
NC_000011.8:g.17613355G= NCBI36
NG_033191.1:g.92860G=
NG_033191.2:g.92860G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.7729+45G= ENSP00000382323.2:n.7729+45G=
ENST00000399397.6:c.7693+45G= MANE Select ENSP00000382329.2:n.7693+45G=
ENST00000342528.2:c.4322-378G= ENSP00000341666.2:n.4322-378G=
ENST00000399391.6:c.7729+45G= ENSP00000382323.2:n.7729+45G=
ENST00000399397.5:c.7693+45G= ENSP00000382329.2:n.7693+45G=
NM_001277269.1:c.7729+45G= NP_001264198.1:n.7729+45G=
NM_001292063.1:c.7693+45G= NP_001278992.1:n.7693+45G=
NM_001277269.2:c.7729+45G= NP_001264198.1:n.7729+45G=
NM_001292063.2:c.7693+45G= MANE Select NP_001278992.1:n.7693+45G=