Canonical Allele Identifier: CA2612690046
Gene: OTOG HGNC NCBI

Linked Data

gnomAD v4: 11-17635026-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17635026A>T , CM000673.2:g.17635026A>T GRCh38
NC_000011.9:g.17656573A>T , CM000673.1:g.17656573A>T GRCh37
NC_000011.8:g.17613149A>T NCBI36
NG_033191.1:g.92654A>T
NG_033191.2:g.92654A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.7622-54A>T ENSP00000382323.2:n.7622-54A>T
ENST00000399397.6:c.7586-54A>T MANE Select ENSP00000382329.2:n.7586-54A>T
ENST00000342528.2:c.4322-584A>T ENSP00000341666.2:n.4322-584A>T
ENST00000399391.6:c.7622-54A>T ENSP00000382323.2:n.7622-54A>T
ENST00000399397.5:c.7586-54A>T ENSP00000382329.2:n.7586-54A>T
NM_001277269.1:c.7622-54A>T NP_001264198.1:n.7622-54A>T
NM_001292063.1:c.7586-54A>T NP_001278992.1:n.7586-54A>T
NM_001277269.2:c.7622-54A>T NP_001264198.1:n.7622-54A>T
NM_001292063.2:c.7586-54A>T MANE Select NP_001278992.1:n.7586-54A>T
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