Canonical Allele Identifier: CA1955232910
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17612360C= , CM000673.2:g.17612360C= GRCh38
NC_000011.9:g.17633907C= , CM000673.1:g.17633907C= GRCh37
NC_000011.8:g.17590483C= NCBI36
NG_033191.1:g.69988C=
NG_033191.2:g.69988C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.6328+30C= ENSP00000382323.2:n.6328+30C=
ENST00000399397.6:c.6292+30C= MANE Select ENSP00000382329.2:n.6292+30C=
ENST00000342528.2:c.3346+30C= ENSP00000341666.2:n.3346+30C=
ENST00000399391.6:c.6328+30C= ENSP00000382323.2:n.6328+30C=
ENST00000399397.5:c.6292+30C= ENSP00000382329.2:n.6292+30C=
NM_001277269.1:c.6328+30C= NP_001264198.1:n.6328+30C=
NM_001292063.1:c.6292+30C= NP_001278992.1:n.6292+30C=
NM_001277269.2:c.6328+30C= NP_001264198.1:n.6328+30C=
NM_001292063.2:c.6292+30C= MANE Select NP_001278992.1:n.6292+30C=