Canonical Allele Identifier: CA1955205813
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17570131G= , CM000673.2:g.17570131G= GRCh38
NC_000011.9:g.17591678G= , CM000673.1:g.17591678G= GRCh37
NC_000011.8:g.17548254G= NCBI36
NG_033191.1:g.27759G=
NG_033191.2:g.27759G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.1814-82G= ENSP00000382323.2:n.1814-82G=
ENST00000399397.6:c.1778-82G= MANE Select ENSP00000382329.2:n.1778-82G=
ENST00000399391.6:c.1814-82G= ENSP00000382323.2:n.1814-82G=
ENST00000399397.5:c.1778-82G= ENSP00000382329.2:n.1778-82G=
ENST00000498332.5:n.1684-82G=
NM_001277269.1:c.1814-82G= NP_001264198.1:n.1814-82G=
NM_001292063.1:c.1778-82G= NP_001278992.1:n.1778-82G=
NM_001277269.2:c.1814-82G= NP_001264198.1:n.1814-82G=
NM_001292063.2:c.1778-82G= MANE Select NP_001278992.1:n.1778-82G=