Canonical Allele Identifier: CA1955240418
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17642137C= , CM000673.2:g.17642137C= GRCh38
NC_000011.9:g.17663684C= , CM000673.1:g.17663684C= GRCh37
NC_000011.8:g.17620260C= NCBI36
NG_033191.1:g.99765C=
NG_033191.2:g.99765C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.8342C= ENSP00000382323.2:p.Ser2781=
ENST00000399397.6:c.8306C= MANE Select ENSP00000382329.2:p.Ser2769=
ENST00000399391.6:c.8342C= ENSP00000382323.2:p.Ser2781=
ENST00000399397.5:c.8306C= ENSP00000382329.2:p.Ser2769=
NM_001277269.1:c.8342C= NP_001264198.1:p.Ser2781=
NM_001292063.1:c.8306C= NP_001278992.1:p.Ser2769=
NM_001277269.2:c.8342C= NP_001264198.1:p.Ser2781=
NM_001292063.2:c.8306C= MANE Select NP_001278992.1:p.Ser2769=