Canonical Allele Identifier: CA1955197704
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553308C= , CM000673.2:g.17553308C= GRCh38
NC_000011.9:g.17574855C= , CM000673.1:g.17574855C= GRCh37
NC_000011.8:g.17531431C= NCBI36
NG_033191.1:g.10936C=
NG_033191.2:g.10936C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.422-57C= ENSP00000382323.2:n.422-57C=
ENST00000399397.6:c.386-57C= MANE Select ENSP00000382329.2:n.386-57C=
ENST00000399391.6:c.422-57C= ENSP00000382323.2:n.422-57C=
ENST00000399397.5:c.386-57C= ENSP00000382329.2:n.386-57C=
ENST00000428619.1:c.203-57C= ENSP00000399057.2:n.203-57C=
ENST00000498332.5:n.292-57C=
NM_001277269.1:c.422-57C= NP_001264198.1:n.422-57C=
NM_001292063.1:c.386-57C= NP_001278992.1:n.386-57C=
NM_001277269.2:c.422-57C= NP_001264198.1:n.422-57C=
NM_001292063.2:c.386-57C= MANE Select NP_001278992.1:n.386-57C=