Canonical Allele Identifier: CA2612679914
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553609_17553611del , CM000673.2:g.17553609_17553611del GRCh38
NC_000011.9:g.17575156_17575158del , CM000673.1:g.17575156_17575158del GRCh37
NC_000011.8:g.17531732_17531734del NCBI36
NG_033191.1:g.11237_11239del
NG_033191.2:g.11237_11239del

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.576+90_576+92del ENSP00000382323.2:n.576+90_576+92del
ENST00000399397.6:c.540+90_540+92del MANE Select ENSP00000382329.2:n.540+90_540+92del
ENST00000399391.6:c.576+90_576+92del ENSP00000382323.2:n.576+90_576+92del
ENST00000399397.5:c.540+90_540+92del ENSP00000382329.2:n.540+90_540+92del
ENST00000498332.5:n.446+90_446+92del
NM_001277269.1:c.576+90_576+92del NP_001264198.1:n.576+90_576+92del
NM_001292063.1:c.540+90_540+92del NP_001278992.1:n.540+90_540+92del
NM_001277269.2:c.576+90_576+92del NP_001264198.1:n.576+90_576+92del
NM_001292063.2:c.540+90_540+92del MANE Select NP_001278992.1:n.540+90_540+92del