Canonical Allele Identifier: CA13478916

Gene: OTOG

Linked Data

• ClinVar Variation Id: 682945
• ClinVar RCV Id: RCV000843091
• dbSNP Id: rs76583012
• gnomAD v2: 11-17633931-G-A
• gnomAD v3: 11-17612384-G-A
• gnomAD v4: 11-17612384-G-A
• MyVariant Identifiers: chr11:g.17633931G>A (hg19) ; chr11:g.17612384G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612384G>A , CM000673.2:g.17612384G>A	GRCh38
NC_000011.9:g.17633931G>A , CM000673.1:g.17633931G>A	GRCh37
NC_000011.8:g.17590507G>A	NCBI36
NG_033191.1:g.70012G>A
NG_033191.2:g.70012G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6328+54G>A	ENSP00000382323.2:n.6328+54G>A
ENST00000399397.6:c.6292+54G>A MANE Select	ENSP00000382329.2:n.6292+54G>A
ENST00000342528.2:c.3346+54G>A	ENSP00000341666.2:n.3346+54G>A
ENST00000399391.6:c.6328+54G>A	ENSP00000382323.2:n.6328+54G>A
ENST00000399397.5:c.6292+54G>A	ENSP00000382329.2:n.6292+54G>A
NM_001277269.1:c.6328+54G>A	NP_001264198.1:n.6328+54G>A
NM_001292063.1:c.6292+54G>A	NP_001278992.1:n.6292+54G>A
NM_001277269.2:c.6328+54G>A	NP_001264198.1:n.6328+54G>A
NM_001292063.2:c.6292+54G>A MANE Select	NP_001278992.1:n.6292+54G>A