Canonical Allele Identifier: CA2612680003

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553644-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553647del , CM000673.2:g.17553647del	GRCh38
NC_000011.9:g.17575194del , CM000673.1:g.17575194del	GRCh37
NC_000011.8:g.17531770del	NCBI36
NG_033191.1:g.11275del
NG_033191.2:g.11275del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.576+128del	ENSP00000382323.2:n.576+128del
ENST00000399397.6:c.540+128del MANE Select	ENSP00000382329.2:n.540+128del
ENST00000399391.6:c.576+128del	ENSP00000382323.2:n.576+128del
ENST00000399397.5:c.540+128del	ENSP00000382329.2:n.540+128del
ENST00000498332.5:n.446+128del
NM_001277269.1:c.576+128del	NP_001264198.1:n.576+128del
NM_001292063.1:c.540+128del	NP_001278992.1:n.540+128del
NM_001277269.2:c.576+128del	NP_001264198.1:n.576+128del
NM_001292063.2:c.540+128del MANE Select	NP_001278992.1:n.540+128del