Canonical Allele Identifier: CA2612686556

Gene: OTOG

Linked Data

• gnomAD v4: 11-17612418-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612418_17612419insA , CM000673.2:g.17612418_17612419insA	GRCh38
NC_000011.9:g.17633965_17633966insA , CM000673.1:g.17633965_17633966insA	GRCh37
NC_000011.8:g.17590541_17590542insA	NCBI36
NG_033191.1:g.70046_70047insA
NG_033191.2:g.70046_70047insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6328+88_6328+89insA	ENSP00000382323.2:n.6328+88_6328+89insA
ENST00000399397.6:c.6292+88_6292+89insA MANE Select	ENSP00000382329.2:n.6292+88_6292+89insA
ENST00000342528.2:c.3346+88_3346+89insA	ENSP00000341666.2:n.3346+88_3346+89insA
ENST00000399391.6:c.6328+88_6328+89insA	ENSP00000382323.2:n.6328+88_6328+89insA
ENST00000399397.5:c.6292+88_6292+89insA	ENSP00000382329.2:n.6292+88_6292+89insA
NM_001277269.1:c.6328+88_6328+89insA	NP_001264198.1:n.6328+88_6328+89insA
NM_001292063.1:c.6292+88_6292+89insA	NP_001278992.1:n.6292+88_6292+89insA
NM_001277269.2:c.6328+88_6328+89insA	NP_001264198.1:n.6328+88_6328+89insA
NM_001292063.2:c.6292+88_6292+89insA MANE Select	NP_001278992.1:n.6292+88_6292+89insA