Canonical Allele Identifier: CA1955197703
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553303A= , CM000673.2:g.17553303A= GRCh38
NC_000011.9:g.17574850A= , CM000673.1:g.17574850A= GRCh37
NC_000011.8:g.17531426A= NCBI36
NG_033191.1:g.10931A=
NG_033191.2:g.10931A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.422-62A= ENSP00000382323.2:n.422-62A=
ENST00000399397.6:c.386-62A= MANE Select ENSP00000382329.2:n.386-62A=
ENST00000399391.6:c.422-62A= ENSP00000382323.2:n.422-62A=
ENST00000399397.5:c.386-62A= ENSP00000382329.2:n.386-62A=
ENST00000428619.1:c.203-62A= ENSP00000399057.2:n.203-62A=
ENST00000498332.5:n.292-62A=
NM_001277269.1:c.422-62A= NP_001264198.1:n.422-62A=
NM_001292063.1:c.386-62A= NP_001278992.1:n.386-62A=
NM_001277269.2:c.422-62A= NP_001264198.1:n.422-62A=
NM_001292063.2:c.386-62A= MANE Select NP_001278992.1:n.386-62A=