Canonical Allele Identifier: CA379811132
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553385A>T , CM000673.2:g.17553385A>T GRCh38
NC_000011.9:g.17574932A>T , CM000673.1:g.17574932A>T GRCh37
NC_000011.8:g.17531508A>T NCBI36
NG_033191.1:g.11013A>T
NG_033191.2:g.11013A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.442A>T ENSP00000382323.2:p.Arg148Trp
ENST00000399397.6:c.406A>T MANE Select ENSP00000382329.2:p.Arg136Trp
ENST00000399391.6:c.442A>T ENSP00000382323.2:p.Arg148Trp
ENST00000399397.5:c.406A>T ENSP00000382329.2:p.Arg136Trp
ENST00000428619.1:c.223A>T ENSP00000399057.2:p.Arg75Trp
ENST00000498332.5:n.312A>T
NM_001277269.1:c.442A>T NP_001264198.1:p.Arg148Trp
NM_001292063.1:c.406A>T NP_001278992.1:p.Arg136Trp
NM_001277269.2:c.442A>T NP_001264198.1:p.Arg148Trp
NM_001292063.2:c.406A>T MANE Select NP_001278992.1:p.Arg136Trp