Canonical Allele Identifier: CA1955233083
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17612687G= , CM000673.2:g.17612687G= GRCh38
NC_000011.9:g.17634234G= , CM000673.1:g.17634234G= GRCh37
NC_000011.8:g.17590810G= NCBI36
NG_033191.1:g.70315G=
NG_033191.2:g.70315G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.6396G= ENSP00000382323.2:p.Lys2132=
ENST00000399397.6:c.6360G= MANE Select ENSP00000382329.2:p.Lys2120=
ENST00000342528.2:c.3414G= ENSP00000341666.2:p.Lys1138=
ENST00000399391.6:c.6396G= ENSP00000382323.2:p.Lys2132=
ENST00000399397.5:c.6360G= ENSP00000382329.2:p.Lys2120=
NM_001277269.1:c.6396G= NP_001264198.1:p.Lys2132=
NM_001292063.1:c.6360G= NP_001278992.1:p.Lys2120=
NM_001277269.2:c.6396G= NP_001264198.1:p.Lys2132=
NM_001292063.2:c.6360G= MANE Select NP_001278992.1:p.Lys2120=