Canonical Allele Identifier: CA2612686641

Gene: OTOG

Linked Data

• gnomAD v4: 11-17612477-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612477G>A , CM000673.2:g.17612477G>A	GRCh38
NC_000011.9:g.17634024G>A , CM000673.1:g.17634024G>A	GRCh37
NC_000011.8:g.17590600G>A	NCBI36
NG_033191.1:g.70105G>A
NG_033191.2:g.70105G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6329-143G>A	ENSP00000382323.2:n.6329-143G>A
ENST00000399397.6:c.6293-143G>A MANE Select	ENSP00000382329.2:n.6293-143G>A
ENST00000342528.2:c.3347-143G>A	ENSP00000341666.2:n.3347-143G>A
ENST00000399391.6:c.6329-143G>A	ENSP00000382323.2:n.6329-143G>A
ENST00000399397.5:c.6293-143G>A	ENSP00000382329.2:n.6293-143G>A
NM_001277269.1:c.6329-143G>A	NP_001264198.1:n.6329-143G>A
NM_001292063.1:c.6293-143G>A	NP_001278992.1:n.6293-143G>A
NM_001277269.2:c.6329-143G>A	NP_001264198.1:n.6329-143G>A
NM_001292063.2:c.6293-143G>A MANE Select	NP_001278992.1:n.6293-143G>A