Canonical Allele Identifier: CA1564375
Gene: OTOF HGNC NCBI

Linked Data

ClinVar Variation Id: 1806149
ClinVar RCV Id: RCV002470433
dbSNP Id: rs771573829
ExAC: 2:26707421 C / T
gnomAD v2: 2-26707421-C-T
gnomAD v3: 2-26484553-C-T
gnomAD v4: 2-26484553-C-T
MyVariant Identifiers: chr2:g.26707421C>T (hg19) chr2:g.26484553C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26484553C>T , CM000664.2:g.26484553C>T GRCh38
NC_000002.11:g.26707421C>T , CM000664.1:g.26707421C>T GRCh37
NC_000002.10:g.26560925C>T NCBI36
NG_009937.1:g.79146G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1126G>A MANE Select ENSP00000272371.2:p.Asp376Asn
ENST00000272371.6:c.1126G>A ENSP00000272371.2:p.Asp376Asn
ENST00000403946.7:c.1126G>A ENSP00000385255.3:p.Asp376Asn
NM_001287489.1:c.1126G>A NP_001274418.1:p.Asp376Asn
NM_194248.2:c.1126G>A NP_919224.1:p.Asp376Asn
XM_005264644.2:c.1171G>A XP_005264701.1:p.Asp391Asn
XM_011533185.1:c.1171G>A XP_011531487.1:p.Asp391Asn
XM_017005338.1:c.1126G>A XP_016860827.1:p.Asp376Asn
NM_001287489.2:c.1126G>A NP_001274418.1:p.Asp376Asn
NM_194248.3:c.1126G>A MANE Select NP_919224.1:p.Asp376Asn
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