Canonical Allele Identifier: CA2574771452
Gene: OTOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17642097G>T , CM000673.2:g.17642097G>T GRCh38
NC_000011.9:g.17663644G>T , CM000673.1:g.17663644G>T GRCh37
NC_000011.8:g.17620220G>T NCBI36
NG_033191.1:g.99725G>T
NG_033191.2:g.99725G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.8332-30G>T ENSP00000382323.2:n.8332-30G>T
ENST00000399397.6:c.8296-30G>T MANE Select ENSP00000382329.2:n.8296-30G>T
ENST00000399391.6:c.8332-30G>T ENSP00000382323.2:n.8332-30G>T
ENST00000399397.5:c.8296-30G>T ENSP00000382329.2:n.8296-30G>T
NM_001277269.1:c.8332-30G>T NP_001264198.1:n.8332-30G>T
NM_001292063.1:c.8296-30G>T NP_001278992.1:n.8296-30G>T
NM_001277269.2:c.8332-30G>T NP_001264198.1:n.8332-30G>T
NM_001292063.2:c.8296-30G>T MANE Select NP_001278992.1:n.8296-30G>T