Canonical Allele Identifier: CA218478389

Gene: OTOG

Linked Data

• dbSNP Id: rs35447294
• MyVariant Identifiers: chr11:g.17633891_17633892insA (hg19) ; chr11:g.17612344_17612345insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612344_17612345insA , CM000673.2:g.17612344_17612345insA	GRCh38
NC_000011.9:g.17633891_17633892insA , CM000673.1:g.17633891_17633892insA	GRCh37
NC_000011.8:g.17590467_17590468insA	NCBI36
NG_033191.1:g.69972_69973insA
NG_033191.2:g.69972_69973insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6328+14_6328+15insA	ENSP00000382323.2:n.6328+14_6328+15insA
ENST00000399397.6:c.6292+14_6292+15insA MANE Select	ENSP00000382329.2:n.6292+14_6292+15insA
ENST00000342528.2:c.3346+14_3346+15insA	ENSP00000341666.2:n.3346+14_3346+15insA
ENST00000399391.6:c.6328+14_6328+15insA	ENSP00000382323.2:n.6328+14_6328+15insA
ENST00000399397.5:c.6292+14_6292+15insA	ENSP00000382329.2:n.6292+14_6292+15insA
NM_001277269.1:c.6328+14_6328+15insA	NP_001264198.1:n.6328+14_6328+15insA
NM_001292063.1:c.6292+14_6292+15insA	NP_001278992.1:n.6292+14_6292+15insA
NM_001277269.2:c.6328+14_6328+15insA	NP_001264198.1:n.6328+14_6328+15insA
NM_001292063.2:c.6292+14_6292+15insA MANE Select	NP_001278992.1:n.6292+14_6292+15insA