Canonical Allele Identifier: CA1955197585
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553101T= , CM000673.2:g.17553101T= GRCh38
NC_000011.9:g.17574648T= , CM000673.1:g.17574648T= GRCh37
NC_000011.8:g.17531224T= NCBI36
NG_033191.1:g.10729T=
NG_033191.2:g.10729T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.329-18T= ENSP00000382323.2:n.329-18T=
ENST00000399397.6:c.293-18T= MANE Select ENSP00000382329.2:n.293-18T=
ENST00000399391.6:c.329-18T= ENSP00000382323.2:n.329-18T=
ENST00000399397.5:c.293-18T= ENSP00000382329.2:n.293-18T=
ENST00000428619.1:c.110-18T= ENSP00000399057.2:n.110-18T=
ENST00000498332.5:n.199-18T=
NM_001277269.1:c.329-18T= NP_001264198.1:n.329-18T=
NM_001292063.1:c.293-18T= NP_001278992.1:n.293-18T=
NM_001277269.2:c.329-18T= NP_001264198.1:n.329-18T=
NM_001292063.2:c.293-18T= MANE Select NP_001278992.1:n.293-18T=