Canonical Allele Identifier: CA1564262
Gene: OTOF HGNC NCBI

Linked Data

ClinVar Variation Id: 597789
dbSNP Id: rs150834957
gnomAD v2: 2-26705382-G-A
gnomAD v3: 2-26482514-G-A
gnomAD v4: 2-26482514-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482514G>A , CM000664.2:g.26482514G>A GRCh38
NC_000002.11:g.26705382G>A , CM000664.1:g.26705382G>A GRCh37
NC_000002.10:g.26558886G>A NCBI36
NG_009937.1:g.81185C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1471C>T MANE Select ENSP00000272371.2:p.Leu491Phe
ENST00000272371.6:c.1471C>T ENSP00000272371.2:p.Leu491Phe
ENST00000403946.7:c.1471C>T ENSP00000385255.3:p.Leu491Phe
NM_001287489.1:c.1471C>T NP_001274418.1:p.Leu491Phe
NM_194248.2:c.1471C>T NP_919224.1:p.Leu491Phe
XM_005264644.2:c.1516C>T XP_005264701.1:p.Leu506Phe
XM_011533185.1:c.1516C>T XP_011531487.1:p.Leu506Phe
XM_017005338.1:c.1471C>T XP_016860827.1:p.Leu491Phe
NM_001287489.2:c.1471C>T NP_001274418.1:p.Leu491Phe
NM_194248.3:c.1471C>T MANE Select NP_919224.1:p.Leu491Phe