Canonical Allele Identifier: CA1955233071
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17612668_17612669delinsGC , CM000673.2:g.17612668_17612669delinsGC GRCh38
NC_000011.9:g.17634215_17634216delinsGC , CM000673.1:g.17634215_17634216delinsGC GRCh37
NC_000011.8:g.17590791_17590792delinsGC NCBI36
NG_033191.1:g.70296_70297delinsGC
NG_033191.2:g.70296_70297delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.6377_6378delinsGC ENSP00000382323.2:p.Ser2126=
ENST00000399397.6:c.6341_6342delinsGC MANE Select ENSP00000382329.2:p.Ser2114=
ENST00000342528.2:c.3395_3396delinsGC ENSP00000341666.2:p.Ser1132=
ENST00000399391.6:c.6377_6378delinsGC ENSP00000382323.2:p.Ser2126=
ENST00000399397.5:c.6341_6342delinsGC ENSP00000382329.2:p.Ser2114=
NM_001277269.1:c.6377_6378delinsGC NP_001264198.1:p.Ser2126=
NM_001292063.1:c.6341_6342delinsGC NP_001278992.1:p.Ser2114=
NM_001277269.2:c.6377_6378delinsGC NP_001264198.1:p.Ser2126=
NM_001292063.2:c.6341_6342delinsGC MANE Select NP_001278992.1:p.Ser2114=