Canonical Allele Identifier: CA1955197587
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553105T= , CM000673.2:g.17553105T= GRCh38
NC_000011.9:g.17574652T= , CM000673.1:g.17574652T= GRCh37
NC_000011.8:g.17531228T= NCBI36
NG_033191.1:g.10733T=
NG_033191.2:g.10733T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.329-14T= ENSP00000382323.2:n.329-14T=
ENST00000399397.6:c.293-14T= MANE Select ENSP00000382329.2:n.293-14T=
ENST00000399391.6:c.329-14T= ENSP00000382323.2:n.329-14T=
ENST00000399397.5:c.293-14T= ENSP00000382329.2:n.293-14T=
ENST00000428619.1:c.110-14T= ENSP00000399057.2:n.110-14T=
ENST00000498332.5:n.199-14T=
NM_001277269.1:c.329-14T= NP_001264198.1:n.329-14T=
NM_001292063.1:c.293-14T= NP_001278992.1:n.293-14T=
NM_001277269.2:c.329-14T= NP_001264198.1:n.329-14T=
NM_001292063.2:c.293-14T= MANE Select NP_001278992.1:n.293-14T=