Canonical Allele Identifier: CA1955242341
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17645848G= , CM000673.2:g.17645848G= GRCh38
NC_000011.9:g.17667395G= , CM000673.1:g.17667395G= GRCh37
NC_000011.8:g.17623971G= NCBI36
NG_033191.1:g.103476G=
NG_033191.2:g.103476G=

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.8682G= ENSP00000382323.2:p.Leu2894=
ENST00000399397.6:c.8646G= MANE Select ENSP00000382329.2:p.Leu2882=
ENST00000399391.6:c.8682G= ENSP00000382323.2:p.Leu2894=
ENST00000399397.5:c.8646G= ENSP00000382329.2:p.Leu2882=
NM_001277269.1:c.8682G= NP_001264198.1:p.Leu2894=
NM_001292063.1:c.8646G= NP_001278992.1:p.Leu2882=
NM_001277269.2:c.8682G= NP_001264198.1:p.Leu2894=
NM_001292063.2:c.8646G= MANE Select NP_001278992.1:p.Leu2882=