Canonical Allele Identifier: CA1955240420
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17642145G= , CM000673.2:g.17642145G= GRCh38
NC_000011.9:g.17663692G= , CM000673.1:g.17663692G= GRCh37
NC_000011.8:g.17620268G= NCBI36
NG_033191.1:g.99773G=
NG_033191.2:g.99773G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.8350G= ENSP00000382323.2:p.Ala2784=
ENST00000399397.6:c.8314G= MANE Select ENSP00000382329.2:p.Ala2772=
ENST00000399391.6:c.8350G= ENSP00000382323.2:p.Ala2784=
ENST00000399397.5:c.8314G= ENSP00000382329.2:p.Ala2772=
NM_001277269.1:c.8350G= NP_001264198.1:p.Ala2784=
NM_001292063.1:c.8314G= NP_001278992.1:p.Ala2772=
NM_001277269.2:c.8350G= NP_001264198.1:p.Ala2784=
NM_001292063.2:c.8314G= MANE Select NP_001278992.1:p.Ala2772=